EP1387384A1 - Motif de matériau luminescent,procédés pour sa fabrication et élément photosensible utilisé - Google Patents
Motif de matériau luminescent,procédés pour sa fabrication et élément photosensible utilisé Download PDFInfo
- Publication number
- EP1387384A1 EP1387384A1 EP03024548A EP03024548A EP1387384A1 EP 1387384 A1 EP1387384 A1 EP 1387384A1 EP 03024548 A EP03024548 A EP 03024548A EP 03024548 A EP03024548 A EP 03024548A EP 1387384 A1 EP1387384 A1 EP 1387384A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- phosphor
- resin composition
- photosensitive resin
- composition layer
- containing photosensitive
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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Images
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F1/00—Originals for photomechanical production of textured or patterned surfaces, e.g., masks, photo-masks, reticles; Mask blanks or pellicles therefor; Containers specially adapted therefor; Preparation thereof
- G03F1/54—Absorbers, e.g. of opaque materials
- G03F1/56—Organic absorbers, e.g. of photo-resists
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- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/0005—Production of optical devices or components in so far as characterised by the lithographic processes or materials used therefor
- G03F7/0007—Filters, e.g. additive colour filters; Components for display devices
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J9/00—Apparatus or processes specially adapted for the manufacture, installation, removal, maintenance of electric discharge tubes, discharge lamps, or parts thereof; Recovery of material from discharge tubes or lamps
- H01J9/20—Manufacture of screens on or from which an image or pattern is formed, picked up, converted or stored; Applying coatings to the vessel
- H01J9/22—Applying luminescent coatings
- H01J9/227—Applying luminescent coatings with luminescent material discontinuously arranged, e.g. in dots or lines
- H01J9/2271—Applying luminescent coatings with luminescent material discontinuously arranged, e.g. in dots or lines by photographic processes
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J2211/00—Plasma display panels with alternate current induction of the discharge, e.g. AC-PDPs
- H01J2211/20—Constructional details
- H01J2211/34—Vessels, containers or parts thereof, e.g. substrates
- H01J2211/42—Fluorescent layers
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J2217/00—Gas-filled discharge tubes
- H01J2217/38—Cold-cathode tubes
- H01J2217/49—Display panels, e.g. not making use of alternating current
Definitions
- This invention relates to a photosensitive element and processes for preparing a phosphor pattern using the same.
- PDP plasma display panel
- PDP flat front plate and back plate comprising glass are arranged in parallel with each other and facing to each other, both of the plates are retained at a certain interval by a barrier rib provided therebetween, and PDP has a structure that discharge is effected in a space surrounded with the front plate, the back plate and the barrier rib.
- a phosphor is coated for display, and by discharge, the phosphor emits light by UV ray generated from filler gas, and the light can be recognized by an observer.
- the above phosphor-dispersed slurry solution is liquid so that dispersion failure due to precipitation of the phosphors occurs easily, and the slurry solution also has a drawback that when a liquid photosensitive resist is used in the slurry solution, storage stability is poor due to acceleration of a dark reaction or the like. Further, the printing method such as screen printing is inferior in printing precision so that there are problems that it is difficult to cope with enlargement of a screen of PDP in the future, and others.
- a phosphor-containing photosensitive resin layer of a photosensitive element comprising a photosensitive resin layer containing a phosphor and a support film is embedded in the space of the above substrate for PDP by contact bonding (lamination) under heating, the layer is subjected to imagewise exposure with active light such as UV ray by a photographic method using a negative film, an unexposed portion is removed by a developing solution such as an alkaline aqueous solution, and further unnecessary organic components are removed by calcination to form a phosphor pattern only at a necessary portion.
- a phosphor pattern is formed in the space of the above substrate for PDP, it is not necessary to confirm dispersibility of a phosphor, and storage stability is also excellent as compared with the case of using a phosphor-dispersed slurry solution or paste. Further, the photographic method is used so that a phosphor pattern can be formed with good precision.
- the invention according to Claim 1 is to provide a phosphor pattern in which lowering of apparent luminance in visual recognition from a wide angle of a field of view can be suppressed in PDP.
- the invention according to Claim 2 is to provide a process for preparing a phosphor pattern, in which property of embedding in a space of a substrate having unevenness such as a substrate for PDP (property of forming a phosphor-containing photosensitive resin composition layer on the wall surface of a barrier rib and the bottom of a space of a substrate for PDP) is excellent and a phosphor pattern with high precision and a uniform shape can be formed.
- a substrate for PDP property of forming a phosphor-containing photosensitive resin composition layer on the wall surface of a barrier rib and the bottom of a space of a substrate for PDP
- the invention according to Claim 3 is to provide a process for preparing a phosphor pattern, having excellent operatability in addition to the effects of the invention according to Claim 2.
- the invention according to Claim 4 is to provide a process for preparing a phosphor pattern, having excellent property of suppressing decrease in phosphor-containing photosensitive resin composition layer thickness in addition to the effects of the invention according to Claim 2 or 3.
- the invention according to Claim 10 is to provide a photosensitive element in which property of suppressing edge fusion and property of embedding in a space of a substrate having unevenness such as a substrate for PDP are excellent and a phosphor pattern with high precision and a uniform shape can be formed with good operatability.
- the invention according to Claim 15 is to provide a process for preparing a phosphor pattern, in which operatability, environmental safety and property of embedding in a space of a substrate having unevenness such as a substrate for PDP are excellent and a phosphor pattern with high precision and a uniform shape can be formed.
- the invention according to Claim 16 is to provide a process for preparing a phosphor pattern, having more excellent operatability in addition to the effects of the invention according to Claim 15.
- the invention according to Claim 17 is to provide a process for preparing a phosphor pattern, having excellent property of suppressing decrease in phosphor-containing photosensitive resin composition layer thickness in addition to the effects of the invention according to Claim 15 or 16.
- the invention according to Claim 23 is to provide a process for preparing a phosphor pattern, in which property of embedding in a space of a substrate having unevenness such as a substrate for PDP is excellent and a phosphor pattern with high precision and a uniform shape can be formed.
- the invention according to Claim 24 is to provide a process for preparing a phosphor pattern, having more excellent operatability in addition to the effects of the invention according to Claim 23.
- the invention according to Claim 25 is to provide a process for preparing a phosphor pattern, having excellent property of suppressing decrease in phosphor-containing photosensitive resin composition layer thickness in addition to the effects of the invention according to Claim 23 or 24.
- the invention according to Claim 29 is to provide a photosensitive element in which property of suppressing edge fusion and property of embedding in a space of a substrate having unevenness such as a substrate for PDP are excellent and a phosphor pattern with high precision and a uniform shape can be formed with good operatability.
- the invention according to Claim 33 is to provide a process for preparing a phosphor pattern, in which property of embedding in a space of a substrate having unevenness such as a substrate for PDP is excellent and a phosphor pattern with high precision and a uniform shape can be formed.
- the invention according to Claim 34 is to provide a process for preparing a phosphor pattern, having more excellent operatability in addition to the effects of the invention according to Claim 33.
- the invention according to Claim 35 is to provide a process for preparing a phosphor pattern, having excellent property of suppressing decrease in phosphor-containing photosensitive resin composition layer thickness in addition to the effects of the invention according to Claim 33 or 34.
- the invention according to Claim 39 is to provide a process for preparing a phosphor pattern, in which property of embedding in a space of a substrate having unevenness such as a substrate for PDP is excellent and a phosphor pattern with high precision and a uniform shape can be formed.
- the invention according to Claim 40 is to provide a process for preparing a phosphor pattern, having more excellent operatability in addition to the effects of the invention according to Claim 39.
- the invention according to Claim 41 is to provide a process for preparing a phosphor pattern, having excellent property of suppressing decrease in phosphor-containing photosensitive resin composition layer thickness in addition to the effects of the invention according to Claim 39 or 40.
- the inventions according to Claims 5, 11, 18, 26, 30, 36 and 42 are to provide a process for preparing a phosphor pattern, having more excellent operatability in addition to the effects of the invention according to Claims 2 to 4, 15 to 17, 23 to 25, 33 to 35 or 39 to 41, and a photosensitive element having more excellent operatability in addition to the effects of the invention according to Claim 10 or 29.
- the inventions according to Claims 6, 12, 19, 27, 31, 37 and 43 are to provide a process for preparing a phosphor pattern, having more excellent storage stability in addition to the effects of the invention according to Claims 2 to 4, 15 to 17, 23 to 25, 33 to 35 or 39 to 41, and a photosensitive element having more excellent storage stability in addition to the effects of the invention according to Claim 10 or 29.
- the inventions according to Claims 7, 13 and 20 are to provide a process for preparing a phosphor pattern, having excellent property of suppressing mixing of colors in addition to the effects of the invention according to Claims 2 to 4 or 15 to 17, and a photosensitive element having more excellent property of suppressing mixing of colors in addition to the effects of the invention according to Claim 10.
- the inventions according to Claims 8 and 21 are to provide a process for preparing a phosphor pattern, having more excellent operatability in addition to the effects of the invention according to Claims 2 to 4 or 15 to 17.
- the inventions according to Claims 9, 14 and 22 are to provide a process for preparing a phosphor pattern, which can form a phosphor pattern with high precision and a uniform shape and has the effects of the invention according to Claims 2 to 4 or 15 to 17, and a photosensitive element which can form a phosphor pattern with high precision and a uniform shape and has the effects of the invention according to Claim 10.
- the inventions according to Claims 28, 32 and 38 are to provide a process for preparing a phosphor pattern, which can form a phosphor pattern with high precision and a uniform shape and has the effects of the invention according to Claims 23 to 25 or 33 to 35, and a photosensitive element which can form a phosphor pattern with high precision and a uniform shape and has the effects of the invention according to Claim 29.
- the phosphor pattern of the present invention comprises a substrate having unevenness and a phosphor layer formed on the inner surface of a concave portion of the substrate, wherein when the length from the bottom of the concave portion to the top of a convex portion is L ( ⁇ m), the phosphor pattern thickness ratio (x)/(y) of the thickness (x) of the phosphor pattern formed on an uneven wall surface at a position of 0.9 x L from the bottom of the concave portion toward the top of the convex portion to the thickness (y). of the phosphor pattern formed on the uneven wall surface at a position of 0.4 x L from the bottom of the concave portion toward the top of the convex portion satisfies a range of 0.1 to 1.5.
- a substrate for a plasma display panel (a substrate for PDP) on which a barrier rib is formed.
- the substrate for PDP there may be mentioned, for example, a substrate such as a glass plate and a synthetic resin plate, which may be subjected to surface treatment for transparent adhesion and on which an electrode and a barrier rib are formed.
- Formation of a barrier rib is not particularly limited, and a known material may be used.
- a rib material containing silica, a thermosetting resin, a low melting point glass (e.g., lead oxide) and a solvent may be used.
- a dielectric film, an insulating film, an auxiliary electrode and a resistor may be formed, if necessary.
- a method for forming the above members on the substrate is not particularly limited.
- an electrode can be formed on the substrate by a method such as vapor deposition, sputtering, plating, coating and printing, and a barrier rib can be formed on the substrate by a method such as a printing method, a sand blasting method and an embedding method.
- Fig. 1 and Fig. 2 each show a schematical view of one embodiment of the substrate for PDP on which a barrier rib is formed.
- the barrier rib generally has a height of 20 to 500 ⁇ m and a width of 20 to 200 ⁇ m.
- the shape of a discharge space surrounded with the barrier rib is not particularly limited and may be lattice-shaped, striped, honeycomb-shaped, triangular or elliptical. In general, a lattice-shaped or striped discharge space as shown in Fig. 1 or Fig. 2 is formed.
- a barrier rib 2 is formed on a substrate 1.
- a lattice-shaped discharge space 3 is formed, and in Fig. 2, a striped discharge space 4 is formed.
- the size of the discharge space is determined by the size and resolution of PDP.
- the longitudinal and lateral lengths are 50 ⁇ m to 1 mm
- the interval is 30 ⁇ m to 1 mm.
- the phosphor layer in the present invention is formed on the bottom of a space of the substrate having unevenness such as the above substrate for PDP and the wall surface of the barrier rib.
- the opening width of the concave portion of such a substrate having unevenness is a narrow opening width such as 80 ⁇ m, 90 ⁇ m, 100 ⁇ m, 120 ⁇ m and 140 ⁇ m, it is preferred to form a phosphor layer or phosphor pattern described below by a photolithographic method described below.
- Fig. 3 shows a state that a phosphor layer 5 is formed on the uneven surface of the substrate 1 for a plasma display panel (the substrate for PDP) on which the barrier rib 2 is formed.
- 6 is a concave portion bottom.
- the phosphor layer in the phosphor pattern of the present invention satisfies that when the length from the concave portion bottom 6 (the surface of the substrate 1) to the top of a convex portion (the barrier rib 2) is L ( ⁇ m), the phosphor pattern thickness ratio (x)/(y) of the thickness (x) of the phosphor pattern formed on an uneven wall surface (the wall surface of the barrier rib 2) at a position of 0.9 x L from the concave portion bottom 6 toward the top of the convex portion to the thickness (y) of the phosphor pattern formed on the uneven wall surface at a position of 0.4 x L from the concave portion bottom 6 toward the top of the convex portion is in the range of 0.1 to 1.5.
- the phosphor pattern thickness ratio (x)/(y) is less than 0.1, when light is emitted as PDP, apparent luminance in visual recognition from a wide angle of a field of view is lowered. On the other hand, it said ratio exceeds 1.5, the utilization rate of visible light emitted by a phosphor is lowered to lower luminance.
- the phosphor pattern thickness ratio (x)/(y) is preferably a ratio satisfying a range of 0.1 to less than 0.5, more preferably a ratio satisfying a range of 0.15 to 0.45, particularly preferably a ratio satisfying a range of 0.2 to 0.4.
- the phosphor pattern thickness ratio (x)/(y) is preferably a ratio satisfying a range of 0.5 to 1.5, more preferably a ratio satisfying a range of 0.55 to 1.3, particularly preferably a ratio satisfying a range of 0.6 to 1.2.
- a process for forming the phosphor pattern (comprising a phosphor layer) of the present invention there may be mentioned, for example, a process including (Ia) a step of heating and pressurizing a thermoplastic resin layer (B) in a state that the layer (B) is superposed on a phosphor-containing photosensitive resin composition layer (A) on an uneven surface of a substrate having unevenness, (IIa) a step of irradiating active light imagewisely, (IIIa) a step of removing unnecessary portions by development and (IVa) a step of removing unnecessary components by calcination.
- the substrate having unevenness in the present invention there may be used, for example, the above substrate for PDP.
- the phosphor-containing photosensitive resin composition layer (A) in the present invention is not particularly limited so long as it is a layer containing a photosensitive resin composition containing a phosphor.
- a layer containing (a) a film property-imparting polymer, (b) a photopolymerizable unsaturated compound having an ethylenic unsaturated group, (c) a photopolymerization initiator which produces free radical by irradiation of active light and (d) a phosphor.
- a vinyl copolymer is preferred.
- a vinyl monomer to be used in the vinyl copolymer there may be mentioned, for example, acrylic acid, methacrylic acid, maleic acid, fumaric acid, itaconic acid, methyl acrylate, methyl methacrylate, ethyl acrylate, ethyl methacrylate, n-propyl acrylate, n-propyl methacrylate, iso-propyl acrylate, iso-propyl methacrylate, n-butyl acrylate, n-butyl methacrylate, iso-butyl acrylate, iso-butyl methacrylate, sec-butyl acrylate, sec-butyl methacrylate, tert-butyl acrylate, tert-butyl methacrylate, pentyl acrylate, pentyl methacrylate, hex
- a polyvinyl alcohol type resin e.g., a hydrolyzate of polyacrylate or polymethacrylate, a hydrolyzate of polyvinyl acetate, a hydrolyzate of a copolymer of ethylene and vinyl acetate, a hydrolyzate of a copolymer of ethylene and acrylate, a hydrolyzate of a copolymer of vinyl chloride and vinyl acetate, a hydrolyzate of a copolymer of styrene and acrylate or methacrylate and a hydrolyzate of a copolymer of vinyltoluene and acrylate or methacrylate), a water-soluble salt of carboxyalkyl cellulose, water-soluble cellulose ethers such as hydroxypropyleneoxy cellulose ether, a water-soluble cellulose such as hydroxypropyloxy cellulose, a water-soluble salt of carboxyal
- the weight average molecular weight (a value obtained by carrying out measurement by gel permeation chromatography and calculated on standard polystyrene) of the film property-imparting polymer (a) in the present invention is preferably 5,000 to 300,000, more preferably 20,000 to 150,000. If the weight average molecular weight is less than 5,000, film-forming property and flexibility tend to be lowered when a photosensitive element is prepared, while if it exceeds 300,000, developability (property that an unnecessary portion can be easily removed by development) tends to be lowered.
- the carboxyl group content (which can be regulated by an acid value (mgKOH/g)) of the film property-imparting polymer (a) can be adjusted suitably.
- the acid value is preferably 90 to 260. If the acid value is less than 90, development tends to be difficult, while if it exceeds 260, developing solution resistance (property that a portion which remains without being removed by development and becomes a pattern is not corroded by a developing solution) tends to be lowered.
- the acid value is preferably 16 to 260. If the acid value is less than 16, development tends to be difficult, while if it exceeds 260, developing solution resistance tends to be lowered.
- a developing solution (an emulsion developing solution) comprising water and at least one organic solvent which is not dissolved in water and when an organic solvent developing solution such as 1,1,1-trichloroethane is used, no carboxyl group may be contained.
- photopolymerizable unsaturated compound (b) having an ethylenic unsaturated group in the present invention there may be used all compounds which have been conventionally known as a photopolymerizable polyfunctional monomer.
- R represents a hydrogen atom or a methyl group
- k represents an integer of 1 to 10
- Y represents a saturated or unsaturated hydrocarbon residue or heterocyclic residue which may have a substituent(s), or a polyalkylene glycol residue
- R 1 represents a hydrogen atom, a methyl group, an ethyl group, a propyl group or a trifluoromethyl group
- m and n each independently represent an integer of 1 to 20.
- the saturated or unsaturated hydrocarbon residue or heterocyclic residue which may have a substituent(s) represented by Y there may be mentioned, for example, a straight, branched or alicyclic alkane residue having 1 to 22 carbon atoms, which may have a substituent(s) such as a halogen atom, a hydroxyl group, an amino group and a carboxyl group (e.g., a methane residue, an ethane residue, a propane residue, a cyclopropane residue, a butane residue, an isobutane residue, a cyclobutane residue, a pentane residue, an isopentane residue, a neopentane residue, a cyclopentane residue, a hexane residue, a cyclohexane residue, a haptane residue, a cycloheptane residue, an octane residue, a non
- an ester type monomer of acrylic acid or methacrylic acid e.g., methyl acrylate, methyl methacrylate, ethyl acrylate, ethyl methacrylate, n-propyl acrylate, n-propyl methacrylate, iso-propyl acrylate, iso-propyl methacrylate, n-butyl acrylate, n-butyl methacrylate, iso-butyl acrylate, iso-butyl methacrylate, sec-butyl acrylate, sec-butyl methacrylate, tert-butyl acrylate, tert-butyl methacrylate, pentyl acrylate, pentyl methacrylate, hexyl acrylate, hexyl methacrylate, heptyl acrylate, heptyl methacrylate,
- ethylene glycol diacrylate ethylene glycol dimethacrylate, diethylene glycol diacrylate, diethylene glycol dimethacrylate, triethylene glycol diacrylate, triethylene glycol dimethacrylate, tetraethylene glycol diacrylate, tetraethylene glycol dimethacrylate, polyethylene glycol diacrylate, polyethylene glycol dimethacrylate, hexapropylene glycol diacrylate, hexapropylene glycol dimethacrylate, polypropylene glycol diacrylate, polypropylene glycol dimethacrylate, polypropylene glycol dimethacrylate, butylene glycol diacrylate, butylene glycol dimethacrylate, neopentyl glycol diacrylate, neopentyl glycol dimethacrylate, 1,3-butanediol diacrylate, 1,3-butanediol dimethacrylate, 1,4-butanediol di
- trimethylolpropane triacrylate trimethylolpropane trimethacrylate, pentaerythritol triacrylate, pentaerythritol trimethacrylate, ethylene oxide-modified trimethylolpropane triacrylate, ethylene oxide-modified trimethylolpropane trimethacrylate, trimethylolpropane triglycidyl ether triacrylate and trimethylolpropane triglycidyl ether trimethacrylate.
- tetramethylolpropane tetraacrylate As a monomer having four unsaturated bonds, there may be mentioned, for example, tetramethylolpropane tetraacrylate, tetramethylolpropane tetramethacrylate, pentaerythritol tetraacrylate and pentaerythritol tetramethacrylate.
- a monomer having five unsaturated bonds there may be mentioned, for example, dipentaerythritol pentaacrylate and dipentaerythritol pentamethacrylate.
- a monomer having six unsaturated bonds there may be mentioned, for example, dipentaerythritol hexaacrylate and dipentaerythritol hexamethacrylate.
- any of these monomers having an unsaturated bond(s) may be used so long as radical polymerization can be effected by irradiation of light, and these monomers having an unsaturated bond(s) are used singly or in combination of two or more of them.
- the weight average molecular weight of the photopolymerizable unsaturated compound (b) having an ethylenic unsaturated group is preferably 400 or more, more preferably 500
- the boiling point (760 mmHg, a found value or a calculated value) of the photopolymerizable unsaturated compound (b) having an ethylenic unsaturated group is not particularly limited so long as it is 300 °C or higher. However, from the points of stability and operatability when heating is carried out under reduced pressure, the boiling point (760 mmHg) is preferably 350 °C or higher, more preferably 400 °C or higher.
- the photopolymerizable unsaturated compound (b) having an ethylenic unsaturated group, having a weight average molecular weight of 400 or more or the photopolymerizable unsaturated compound (b) having an ethylenic unsaturated group, having a boiling point (760 mmHg) of 300 °C or higher may be selected from, for example, photopolymerizable unsaturated compounds shown below.
- an ester type monomer of acrylic acid or methacrylic acid polyethylene glycol acrylate (the number of ethylene oxides is 9 to 50), polyethylene glycol methacrylate (the number of ethylene oxides is 9 to 50), methoxypolyethylene glycol acrylate (the number of ethylene oxides is 9 to 50), methoxypolyethylene glycol methacrylate (the number of ethylene oxides is 9 to 50), methoxypolypropylene glycol acrylate (the number of propylene oxides is 7 to 40), methoxypolypropylene glycol methacrylate (the number of propylene oxides is 7 to 40) or the like), a styrene type monomer, a polyolefin type monomer, a vinyl type monomer and a nitrile type monomer.
- polyethylene glycol diacrylate (the number of ethylene oxides is 9 to 50), polyethylene glycol dimethacrylate (the number of ethylene oxides is 9 to 50), hexapropylene glycol diacrylate, hexapropylene glycol dimethacrylate, polypropylene glycol diacrylate (the number of propylene oxides is 7 to 40), polypropylene glycol dimethacrylate (the number of propylene oxides is 7 to 40), polyethylene glycol polypropylene glycol diacrylate (the total number of ethylene oxides and propylene oxides is 7 to 50), polyethylene glycol polypropylene glycol dimethacrylate (the total number of ethylene oxides and propylene oxides is 7 to 50), 2,2-bis(4-acryloxydiethoxyphenyl)-propane, 2,2-bis(4-methacryloxydiethoxyphenyl)propane, 2,2-bis(4-acryloxy
- a monomer having three unsaturated bonds there may be mentioned, for example, propylene oxide-modified trimethylolpropane trimethacrylate and alkyl-modified dipentaerythritol triacrylate.
- a monomer having four unsaturated bonds there may be mentioned, for example, ditrimethylolpropane tetramethacrylate, alkyl-modified dipentaerythritol tetraacrylate, alkyl-modified dipentaerythritol tetramethacrylate, ethylene oxide-modified pentaerythritol tetraacrylate and ethylene oxide-modified pentaerythritol tetramethacrylate.
- dipentaerythritol pentaacrylate dipentaerythritol pentamethacrylate
- dipentaerythritol monohydroxypentaacrylate dipentaerythritol monohydroxypentamethacrylate
- alkyl-modified dipentaerythritol pentaacrylate dipentaerythritol pentaacrylate
- a monomer having six unsaturated bonds there may be mentioned, for example, dipentaerythritol hexaacrylate and dipentaerythritol hexamethacrylate.
- an aromatic ketone e.g., benzophenone, N,N'-tetramethyl-4,4'-diaminobenzophenone (Michler's ketone), N,N'-tetraethyl-4,4'-diaminobenzophenone, 4-methoxy-4'-dimethylaminobenzophenone, 1-hydroxy-cyclohexyl-phenyl-ketone, 2,4-diethylthioxanthone, 2-ethylanthraquinone and phenanthrenequinone), a benzoin ether (e.g., benzoin methyl ether, benzoin ethyl ether and benzoin phenyl ether), a benzoin (e.g., methyl benzoin and ethyl benzoin), a benzoin (e.g., methyl benzoin and ethyl benzoin), a benzoin (e.g., methyl be
- the phosphor (d) is not particularly limited, and a phosphor comprising a common metal oxide as a main component is used.
- a phosphor which emits red light there may be mentioned, for example, Y 2 O 2 S:Eu, Zn 3 (PO 4 ) 2 :Mn, Y 2 O 3 :Eu, YVO 4 :Eu, (Y,Gd)BO 3 :Eu, ⁇ -Zn 3 (PO 4 ) 2 :Mn and (ZnCd)S:Ag+In 2 O.
- a phosphor which emits green light there may be mentioned, for example, ZnS:Cu, Zn 2 SiO 4 :Mn, ZnS:Cu+Zn 2 SiO 4 :Mn, Gd 2 O 2 S:Tb, Y 3 Al 5 O 12 :Ce, ZnS:Cu,Al, Y 2 O 2 S:Tb, ZnO:Zn, ZnS:Cu,Al+In 2 O 3 , LaPO 4 :Ce,Tb and BaO ⁇ 6Al 2 O 3 :Mn.
- the particle size of the phosphor (d) in the present invention is preferably 0.1 to 20 ⁇ m, more preferably 1 to 15 ⁇ m, particularly preferably 2 to 8 ⁇ m. If the particle size is less than 0.1 ⁇ m, light emission efficiency tends to be lowered, while if it exceeds 20 ⁇ m, dispersibility tends to be lowered.
- the shape of the phosphor (d) in the present invention is preferably spherical, and it is preferred that its surface area is smaller.
- the formulation amount of Component (a) in the present invention is preferably 10 to 90 parts by weight, more preferably 20 to 80 parts by weight based on the total amount of Component (a) and Component (b) being 100 parts by weight. If the formulation amount is less than 10 parts by weight, when the resulting material is supplied as a photosensitive element in a roll state, a phosphor-containing photosensitive resin is exuded from a roll edge portion (hereinafter referred to as "edge fusion") so that it is difficult to carry out drawing from a roll at the time of lamination of a photosensitive element, and an exuded portion is partially and excessively embedded in the space of the substrate for PDP, whereby a problem of significant lowering of production yield is caused or film-forming property tends to be lowered. If the formulation amount exceeds 90 parts by weight, sensitivity tends to be insufficient.
- the formulation amount of Component (b) in the present invention is preferably 10 to 90 parts by weight, more preferably 20 to 80 parts by weight based on the total amount of Component (a) and Component (b) being 100 parts by weight. If the formulation amount is less than 10 parts by weight, the sensitivity of a phosphor-containing photosensitive resin composition tends to be insufficient. If the formulation amount exceeds 90 parts by weight, a photocured product tends to be brittle, and when a photosensitive element is prepared, a phosphor-containing photosensitive resin composition tends to be exuded from an edge portion by flowing, or film-forming property tends to be lowered.
- the formulation amount of Component (c) in the present invention is preferably 0.01 to 30 parts by weight, more preferably 0.1 to 20 parts by weight based on the total amount of Component (a) and Component (b) being 100 parts by weight. If the formulation amount is less than 0.01 part by weight, the sensitivity of a phosphor-containing photosensitive resin composition tends to be insufficient. If the formulation amount exceeds 30 parts by weight, photocuring of an inner portion tends to be insufficient due to increase in absorption of active light at an exposed surface of a phosphor-containing photosensitive resin composition.
- the formulation amount of Component (d) in the present invention is preferably 10 to 400 parts by weight, more preferably 50 to 380 parts by weight based on the total amount of Component (a), Component (b) and Component (c) being 100 parts by weight. If the formulation amount is less than 10 parts by weight, when light is emitted as PDP, light emission efficiency tends to be lowered. If the formulation amount exceeds 400 parts by weight, when a photosensitive element is prepared, film-forming property tends to be lowered, or flexibility tends to be lowered.
- the phosphor-containing photosensitive resin composition layer (A) in the present invention may comprise (e) a photopolymerizable high molecular weight binder having an ethylenic unsaturated group, (f) a photopolymerization initiator which produces free radical by irradiation of active light and (g) a phosphor.
- photopolymerizable high molecular weight binder (e) having an ethylenic unsaturated group there may be mentioned a photopolymerizable vinyl copolymer obtained by subjecting a compound having at least one ethylenic unsaturated group and one functional group such as an oxirane ring, an isocyanate group, a hydroxyl group and a carboxyl group to accition reaction with a vinyl copolymer having a functional group such as a carboxyl group, a hydroxyl group, an amino group, an isocyanate group, an oxirane ring and an acid anhydride.
- a photopolymerizable vinyl copolymer obtained by subjecting a compound having at least one ethylenic unsaturated group and one functional group such as an oxirane ring, an isocyanate group, a hydroxyl group and a carboxyl group to accition reaction with a vinyl copolymer having a functional group such as a carboxyl
- a vinyl monomer to be used in the vinyl copolymer having a functional group such as a carboxyl group, a hydroxyl group, an amino group, an oxirane ring and an acid anhydride there may be mentioned, for example, a vinyl monomer having a functional group such as a carboxyl group, a hydroxyl group, an amino group, an oxirane ring and an acid anhydride, such as acrylic acid, methacrylic acid, maleic acid, fumaric acid, itaconic acid, cinnamic acid, 2-hydroxyethyl acrylate, 2-hydroxyethyl methacrylate, acrylamide, methacrylamide, isocyanate-ethyl methacrylate, glycidyl acrylate, glycidyl methacrylate and maleic anhydride.
- a vinyl monomer having a functional group such as a carboxyl group, a hydroxyl group, an amino group, an oxirane ring and an acid anhydr
- vinyl monomer there may be mentioned, for example, methyl acrylate, methyl methacrylate, ethyl acrylate, ethyl methacrylate, n-propyl acrylate, n-propyl methacrylate, iso-propyl acrylate, iso-propyl methacrylate, n-butyl acrylate, n-butyl methacrylate, iso-butyl acrylate, isobutyl methacrylate, sec-butyl acrylate, sec-butyl methacrylate, tert-butyl acrylate, tert-butyl methacrylate, pentyl acrylate, pentyl methacrylate, hexyl acrylate, hexyl methacrylate, heptyl acrylate, heptyl methacrylate, 2-ethylhexyl acrylate, 2-ethylhexyl methacrylate, o
- These monomers are used singly or in combination of two or more of them with the vinyl monomer having a functional group such as a carboxyl group, a hydroxyl group, an amino group, an oxirane ring and an acid anhydride being an indispensable component.
- a functional group such as a carboxyl group, a hydroxyl group, an amino group, an oxirane ring and an acid anhydride being an indispensable component.
- the compound having at least one ethylenic unsaturated group and one functional group such as an oxirane ring, an isocyanate group, a hydroxyl group, a carboxyl group, an amino group and an acid anhydride there may be mentioned, for example, glycidyl acrylate, glycidyl methacrylate, ethyl isocyanate methacrylate, 2-hydroxyethyl acrylate, 2-hydroxyethyl methacrylate, acrylic acid, methacrylic acid, maleic acid, fumaric acid, itaconic acid, cinnamic acid, acrylamide, methacrylamide and maleic anhydride.
- These compounds are used singly or in combination of two or more of them.
- the weight average molecular weight of the photopolymerizable high molecular weight binder (e) having an ethylenic unsaturated group is preferably 5,000 to 300,000, more preferably 20,000 to 150,000. If the weight average molecular weight is less than 5,000, when a photosensitive element is prepared, film-forming property and flexibility tend to be lowered, while if it exceeds 300,000, developability (property that an unnecessary portion can be easily removed by development) tends to be lowered.
- the carboxyl group content (which can be regulated by an acid value (mgKOH/g)) of the photopolymerizable high molecular weight binder (e) having an ethylenic unsaturated group can be adjusted suitably.
- the acid value is preferably 90 to 260. If the acid value is less than 90, development tends to be difficult, while if it exceeds 260, developing solution resistance (property that a portion which remains without being removed by development and becomes a pattern is not corroded by a developing solution) tends to be lowered.
- the acid value is preferably 16 to 260. If the acid value is less than 16, development tends to be difficult, while if it exceeds 260, developing solution resistance tends to be lowered.
- a developing solution (an emulsion developing solution) comprising water and at least one organic solvent which is not dissolved in water and when an organic solvent developing solution such as 1,1,1-trichloroethane is used, no carboxyl group may be contained.
- the concentration of the ethylenic unsaturated group of the photopolymerizable high molecular weight binder (e) having an ethylenic unsaturated group is preferably 3.0 x 10 -4 to 5.8 x 10 -3 mol/g, more preferably 6.0 x 10 -4 to 5.5 x 10 -3 mol/g, particularly preferably 9 x 10 -4 to 5.0 x 10 -3 mol/g.
- concentration of the ethylenic unsaturated group is less than 3.0 x 10 -4 mol/g, developing solution resistance (property that a portion which remains without being removed by development and becomes a pattern is not corroded by a developing solution) tends to be lowered, while if it exceeds 5.8 x 10 -3 mol/g, gelation tends to occur during preparation of the photopolymerizable high molecular weight binder (e) having an ethylenic unsaturated group.
- the photopolymerization initiator (f) which produces free radical by irradiation of active light in the present invention there may be used, for example, the above photopolymerization initiator (c) which produces free radical by irradiation of active light, which can be used in the photosensitive resin composition constituting the phosphor-containing photosensitive resin composition layer (A).
- photopolymerization initiators are used singly or in combination of two or more of them.
- the phosphor (g) in the present invention is not particularly limited, and there may be used the above phosphor (d) which can be used in the photosensitive resin composition constituting the phosphor-containing photosensitive resin composition layer (A).
- the formulation amount of Component (f) in the present invention is preferably 0.01 to 30 parts by weight, more preferably 0.1 to 20 parts by weight based on 100 parts by weight of Component (e). If the formulation amount is less than 0.01 part by weight, the sensitivity of a phosphor-containing photosensitive resin composition tends to be insufficient, while if it exceeds 30 parts by weight, photocuring of an inner portion tends to be insufficient due to increase in absorption of active light at an exposed surface of a phosphor-containing photosensitive resin composition.
- the formulation amount of Component (g) in the present invention is preferably 10 to 400 parts by weight, more preferably 50 to 380 parts by weight, particularly preferably 70 to 350 parts by weight based on 100 parts by weight of Component (e). If the formulation amount is less than 10 parts by weight, when light is emitted as PDP, light emission efficiency tends to be lowered. If the formulation amount exceeds 400 parts by weight, when a photosensitive element is prepared, film-forming property tends to be lowered, or flexibility tends to be lowered.
- the photopolymerization initiator (f) which produces free radical by irradiation of active light and the phosphor (g) in the present invention
- a photopolymerizable unsaturated compound having an ethylenic unsaturated group may be used when a photosensitive element is prepared and in such a formulation amount range that storage stability (property that a phenomenon that the photopolymerizable unsaturated compound having an ethylenic unsaturated group in the phosphor-containing photosensitive resin composition layer (A) is migrated into the thermoplastic resin layer (B) described below is suppressed, and the thermoplastic resin layer (B) is not photocured thereby) after embedding in the space of the substrate for PDP can be maintained.
- the photopolymerizable unsaturated compound having an ethylenic unsaturated group there may be mentioned, for example, the above photopolymerizable unsaturated compound (b) having an ethylenic unsaturated group, which can be used in the photosensitive resin composition constituting the phosphor-containing photosensitive resin composition layer (A). These compounds are used singly or in combination of two or more of them.
- the formulation amount of the photopolymerizable unsaturated compound having an ethylenic unsaturated group, which can be used in the phosphor-containing photosensitive resin composition layer (A) constituted by the photopolymerizable high molecular weight binder (e) having an ethylenic unsaturated group, the photopolymerization initiator (f) which produces free radical by irradiation of active light and the phosphor (g) in the present invention is preferably 1 to 80 parts by weight, more preferably 3 to 70 parts by weight, particularly preferably 5 to 60 parts by weight based on the total amount of Component (e) and the photopolymerizable unsaturated compound having an ethylenic unsaturated group being 100 parts by weight. If the formulation amount is less than 1 part by weight, when a photosensitive element is prepared, film-forming property tends to be lowered. If the formulation amount exceeds 80 parts by weight, developing solution resistance tends to be lowered.
- the photopolymerization initiator (f) which produces free radical by irradiation of active light and the phosphor (g) in the present invention
- a film property-imparting polymer may be used.
- the film property-imparting polymer there may be used, for example, the above film property-imparting polymer (a) which can be used in the photosensitive resin composition constituting the phosphor-containing photosensitive resin composition layer (A). These polymers are used singly or in combination of two or more of them.
- the formulation amount of the film property-imparting polymer which can be used in the phosphor-containing photosensitive resin composition layer (A) constituted by the photopolymerizable high molecular weight binder (e) having an ethylenic unsaturated group, the photopolymerization initiator (f) which produces free radical by irradiation of active light and the phosphor (g) in the present invention is preferably 1 to 80 parts by weight, more preferably 3 to 70 parts by weight, particularly preferably 5 to 60 parts by weight based on the total amount of Component (e) and the film property-imparting polymer being 100 parts by weight. If the formulation amount is less than 1 part by weight, when a photosensitive element is prepared, no effect of improving flexibility tends to be obtained. If the formulation amount exceeds 80 parts by weight, sensitivity tends to be lowered.
- a compound having a carboxyl group may be contained in order to prevent thickening for a long period of time and obtain good storage stability.
- the compound having a carboxyl group there may be mentioned, for example, a saturated aliphatic acid, an unsaturated aliphatic acid, an aliphatic dibasic acid, an aromatic dibasic acid, an aliphatic tribasic acid and an aromatic tribasic acid.
- formic acid acetic acid, chloroacetic acid, dichloroacetic acid, trichloroacetic acid, propionic acid capric acid, undecanoic acid, lauric acid, tridecanoic acid, myristic acid, pentadecanoic acid, palmitic acid, heptadecanoic acid, stearic acid, nonadecanoic acid, arachidic acid, palmitoleic acid, oleic acid, elaidic acid, linolenic acid, linoleic acid, oxalic acid, malonic acid, methylmalonic acid, ethylmalonic acid, monomethyl malonate, monoethyl malonate, succinic acid, methylsuccinic acid, adipic acid, methyladipic acid, pimelic acid, suberic acid, azelaic acid, sebacic acid, maleic acid, itaconic acid,
- oxalic acid, malonic acid, methylmalonic acid, ethylmalonic acid and citric acid are preferred, and oxalic acid, malonic acid and citric acid are more preferred. These compounds are used singly or in combination of two or more of them.
- the formulation amount of the compound having a carboxyl group is preferably 0.01 to 30 parts by weight based on 100 parts by weight of Component (a) or Component (e). If the formulation amount is less than 0.01 part by weight, an effect of storage stability tends to be lowered, while if it exceeds 30 parts by weight, sensitivity tends to be insufficient.
- a dispersant to the photosensitive resin composition constituting the phosphor-containing photosensitive resin composition layer (A) in the present invention.
- an inorganic dispersant e.g., silica gel type, bentonite type, kaolinite type, talc type, hectorite type, montmorillonite type, saponite type and beidellite type
- an organic dispersant e.g., aliphatic acid amide type, aliphatic acid ester type, polyethylene oxide type, a sulfate type anion surfactant, polycarboxylic acid amine salt type, polycarboxylic acid type, polyamide type, high molecular weight polyether type, acryl copolymer type and special silicone type.
- the amount of the dispersant to be used is not particularly limited, but it is preferably 0.01 to 100 parts by weight based on 100 parts by weight of Component (a) or Component (e). If the amount to be used is less than 0.01 part by weight, an effect to be brought about by addition tends not to appear, while if it exceeds 100 parts by weight, precision of pattern formation (property that a pattern comprising a phosphor-containing photosensitive resin composition can be obtained with dimensional precision and a desired shape after development) tends to be lowered.
- the photosensitive resin composition constituting the phosphor-containing photosensitive resin composition layer (A) in the present invention it is preferred to use a binding agent for the purpose of preventing peeling of the phosphor from the substrate for PDP after calcination.
- binding agent there may be mentioned, for example, a low melting point glass, a metal alkoxide and a silane coupling agent. These binding agents are used singly or in combination of two or more of them.
- the amount of the binder to be used is not particularly limited, but it is preferably 0.01 to 100 parts by weight, more preferably 0.05 to 50 parts by weight, particularly preferably 0.1 to 30 parts by weight based on 100 parts by weight of Component (d) or Component (g). If the amount to be used is less than 0.01 part by weight, an effect of binding the phosphor tends not to appear, while if it exceeds 100 parts by weight, light emission efficiency tends to be lowered.
- a plasticizer may be added to the phosphor-containing photosensitive resin composition layer (A) in the present invention.
- R represents a hydrogen atom or a methyl group
- Y 1 represents a hydrogen atom, a saturated hydrocarbon group which may have a substituent(s) or a polyalkylene glycol residue
- Y 2 represents
- the formulation amount of the plasticizer is preferably 10 to 90 parts by weight, more preferably 20 to 80 parts by weight, particularly preferably 30 to 70 parts by weight based on 100 parts by weight of Component (a) or Component (e). If the formulation amount is less than 10 parts by weight, when a photosensitive element is prepared, an effect of film-forming property tends to be low. If the formulation amount exceeds 90 parts by weight, the sensitivity of the phosphor-containing photosensitive resin composition layer (A) tends to be insufficient.
- a dye, a color-forming agent, a pigment, a polymerization inhibitor, a surface-modifying agent, a stabilizer, an adhesiveness-imparting agent and a thermosetting agent may be added to the photosensitive resin composition constituting the phosphor-containing photosensitive resin composition layer (A) in the present invention.
- the photosensitive resin composition other than the phosphor (d), the phosphor (g) and the binding agent in the photosensitive resin composition constituting the phosphor-containing photosensitive resin composition layer (A) in the present invention has good thermal decomposition property. Therefore, it is preferred that the photosensitive resin composition other than the phosphor (d), the phosphor (g) and the binding agent does not contain elements other than carbon, hydrogen, oxygen and nitrogen as elements constituting said composition.
- the phosphor-containing photosensitive resin composition layer (A) in the present invention can be obtained by dissolving the above respective components constituting said layer in or mixing said components with a solvent which can dissolve or disperse said components to prepare a solution in which said components are dispersed uniformly and coating the solution on a support film, followed by drying.
- the solvent which can dissolve or disperse the above respective components constituting the phosphor-containing photosensitive resin composition layer (A) there may be mentioned, for example, toluene, acetone, methyl ethyl ketone, methyl isobutyl ketone, methyl cellosolve, ethyl cellosolve, ⁇ -butyrolactone, N-methylpyrrolidone, dimethylformamide, tetramethylsulfone, diethylene glycol dimethyl ether, diethylene glycol monobutyl ether, chloroform, methylene chloride, methyl alcohol and ethyl alcohol.
- solvents are used singly or in combination of two or more of them.
- the support film there may be mentioned a support film which is chemically and thermally stable and constituted by a flexible substance, for example, polyethylene terephthalate, polycarbonate, polyethylene and polypropylene. Among them, polyethylene terephthalate and polyethylene are preferred, and polyethylene terephthalate is more preferred.
- the support film can be removed later from the phosphor-containing photosensitive resin composition layer (A) so that it should not be a film subjected to surface treatment or comprising a material which makes removing impossible.
- the thickness of the support film is preferably 5 to 100 ⁇ m, more preferably 10 to 90 ⁇ m.
- a coating method a known method may be used, and there may be mentioned, for example, a knife coating method, a roll coating method, a spray coating method, a gravure coating method, a bar coating method and a curtain coating method.
- the material of a portion of a coating apparatus, contacted with the solution in which the above respective components constituting the phosphor-containing photosensitive resin composition layer (A) are dispersed uniformly by dissolving said components in or mixing said components with the solvent which can dissolve or disperse said components is preferably a non-metallic material.
- the coating apparatus contacted with the solution constituting the phosphor-containing photosensitive resin composition layer (A) is polished by the phosphor in said solution, and powder generated by polishing tends to migrate, as impurity, into the solution constituting the phosphor-containing photosensitive resin composition layer (A).
- the drying temperature is preferably 60 to 130 °C, and the drying time is preferably 3 minutes to 1 hour.
- the thickness of the phosphor-containing photosensitive resin composition layer (A) in the present invention is not particularly limited, but it is preferably 10 to 200 ⁇ m, more preferably 15 to 150 ⁇ m, particularly preferably 20 to 100 ⁇ m. If the thickness is less than 10 ⁇ m, a phosphor pattern after calcination described below tends to be thin to lower light emission efficiency, while if it exceeds 200 ⁇ m, a phosphor pattern after calcination tends to be thick to reduce a light emission area of a phosphor surface, which results in lowering of light emission efficiency.
- the viscosity at 100 °C of the phosphor-containing photosensitive resin composition layer (A) in the present invention is preferably 1 to 1 x 10 9 Pa ⁇ sec, more preferably 2 to 1 x 10 8 Pa ⁇ sec, particularly preferably 5 to 1 x 10 7 Pa ⁇ sec, extremely preferably 10 to 1 x 10 6 Pa ⁇ sec. If the viscosity at 100 °C is less than 1 Pa ⁇ sec, the viscosity at room temperature becomes too low so that when a photosensitive element is prepared, the phosphor-containing photosensitive resin composition layer (A) tends to be exuded from an edge portion by flowing, and film-forming property tends to be lowered.
- the number of step tablet grades of the remaining phosphor-containing photosensitive resin composition layer (A) is preferably 1 to 21 grades, more preferably 1.5 to 18 grades, particularly preferably 2 to 15 grades.
- the minimum line/space of the remaining the phosphor-containing photosensitive resin composition layer (A) is preferably 1 mm/1 mm or less, more preferably 900 ⁇ m/900 ⁇ m or less, particularly preferably 800 ⁇ m/800 ⁇ m.
- the minimum line/space of the remaining the phosphor-containing photosensitive resin composition layer (A) is preferably 400 ⁇ m/400 ⁇ m or less, more preferably 350 ⁇ m/400 ⁇ m or less, particularly preferably 300 ⁇ m/400 ⁇ m.
- a peelable cover film may be further laminated.
- cover film there may be mentioned polyethylene, polypropylene, polyethylene terephthalate and polycarbonate. It is preferred that the adhesive strength of the cover film to the phosphor-containing photosensitive resin composition layer (A) is smaller than the adhesive strength of the cover film to the support film.
- the thickness of the cover film is not particularly limited, but it is preferably 5 to 100 ⁇ m, more preferably 10 to 90 ⁇ m.
- the photosensitive element of the present invention obtained as described above can be stored by being wound in a roll state.
- a resin constituting the thermoplastic resin layer (B) in the present invention is not particularly limited so long as it is softened at temperature at the time of contact bonding under heating, and there may be mentioned, for example, polyethylene, polypropylene, polyvinyl chloride, polyvinyl acetate, polyvinylidene chloride, polystyrene, polyvinyltoluene, polyacrylate, polymethacrylate, a copolymer of ethylene and vinyl acetate, a copolymer of ethylene and acrylate, a copolymer of vinyl chloride and vinyl acetate, a copolymer of styrene and acrylate or methacrylate, a copolymer of vinyltoluene and acrylate or methacrylate, a polyvinyl alcohol type resin (e.g., a hydrolyzate of polyacrylate or polymethacrylate, a hydrolyzate of polyvinyl acetate, a hydrolyzate of a
- the thermoplastic resin layer (B) in the present invention may be constituted by a photosensitive resin composition comprising (h) a thermoplastic resin, (i) a photopolymerizable unsaturated compound having an ethylenic unsaturated group and (j) a photopolymerization initiator which produces free radical by irradiation of active light.
- thermoplastic resin (h) there may be used a resin which can be used as the above resin constituting the thermoplastic resin layer (B), and the above film property-imparting polymer (a) which can be used in the photosensitive resin composition constituting the phosphor-containing photosensitive resin composition layer (A).
- the photopolymerizable unsaturated compound (i) having an ethylenic unsaturated group there may be used the above photopolymerizable unsaturated compound (b) having an ethylenic unsaturated group, which can be used in the photosensitive resin composition constituting the phosphor-containing photosensitive resin composition layer (A).
- the photopolymerization initiator (j) which produces free radical by irradiation of active light there may be used the above photopolymerization initiator (c) which produces free radical by irradiation of active light, which can be used in the photosensitive resin composition constituting the phosphor-containing photosensitive resin composition layer (A).
- the formulation amount of Component (h) is preferably 10 to 90 parts by weight, more preferably 20 to 80 parts by weight based on the total amount of Component (h) and Component (i) being 100 parts by weight. If the formulation amount is less than 10 parts by weight, when a photosensitive element is prepared, a photosensitive resin-composition tends to be exuded from an edge portion by flowing, or film-forming property tends to be lowered. If the formulation amount exceeds 90 parts by weight, sensitivity tends to be insufficient.
- the formulation amount of Component (i) is preferably 10 to 90 parts by weight, more preferably 20 to 80 parts by weight based on the total amount of Component (h) and Component (i) being 100 parts by weight. If the formulation amount is less than 10 parts by weight, sensitivity tends to be insufficient, while if it exceeds 90 parts by weight, when a photosensitive element is prepared, a photosensitive resin composition tends to be exuded from an edge portion by flowing, or film-forming property tends to be lowered.
- the formulation amount of Component (j) is preferably 0.01 to 30 parts by weight, more preferably 0.1 to 20 parts by weight based on the total amount of Component (h) and Component (i) being 100 parts by weight. If the formulation amount is less than 0.01 part by weight, sensitivity tends to be insufficient, while if it exceeds 30 parts by weight, photocuring of an inner portion tends to be insufficient due to increase in absorption of active light at an exposed surface.
- thermoplastic resin layer (B) can be developed by using the same developing solution by which the phosphor-containing photosensitive resin composition layer (A) is developed.
- thermoplastic resin layer (B) which can be developed by the same developing solution, there may be mentioned a thermoplastic resin layer which is soluble in water or an alkaline aqueous solution.
- thermoplastic resin layer (B) which is soluble in water or an alkaline aqueous solution
- a polyvinyl alcohol type resin e.g., a hydrolyzate of polyacrylate or polymethacrylate, a hydrolyzate of polyvinyl acetate, a hydrolyzate of a copolymer of ethylene and vinyl acetate, a hydrolyzate of a copolymer of ethylene and acrylate, a hydrolyzate of a copolymer of vinyl chloride and vinyl acetate, a hydrolyzate of a copolymer of styrene and acrylate or methacrylate and a hydrolyzate of a copolymer of vinyltoluene and acrylate or methacrylate), a water-soluble salt of carboxyalkyl cellulose, water-soluble cellulose ethers, a water-soluble salt of carboxyalkyl starch, polyvinyl
- the resin having a carboxyl group obtained by copolymerizing an unsaturated carboxylic acid and an unsaturated monomer which is copolymerizable therewith it is preferred to use, for example, a vinyl copolymer obtained by copolymerizing an unsaturated carboxylic acid (e.g., acrylic acid, methacrylic acid, maleic acid, fumaric acid and itaconic acid) and the above vinyl monomer which can be used in the film property-imparting polymer (a) constituting the phosphor-containing photosensitive resin composition layer (A).
- an unsaturated carboxylic acid e.g., acrylic acid, methacrylic acid, maleic acid, fumaric acid and itaconic acid
- the weight average molecular weight of the resin having a carboxyl group obtained by copolymerizing an unsaturated carboxylic acid and an unsaturated monomer which is copolymerizable therewith is preferably 5,000 to 300,000, more preferably 20,000 to 150,000. If the weight average molecular weight is less than 5,000, when a photosensitive element is prepared, film-forming property and flexibility tend to be lowered, while if it exceeds 300,000, developability tends to be lowered.
- the carboxyl group content (which can be regulated by an acid value (mgKOH/g)) of the resin having a carboxyl group obtained by copolymerizing an unsaturated carboxylic acid and an unsaturated monomer which is copolymerizable therewith can be adjusted suitably.
- the acid value is preferably 90 to 260. If the acid value is less than 90, development tends to be difficult, while if it exceeds 260, developing solution resistance tends to be lowered.
- the acid value is preferably 16 to 260. If the acid value is less than 16, development tends to be difficult, while if it exceeds 260, developing solution resistance tends to be lowered.
- thermoplastic resin layer (B) In order to obtain good film property of the thermoplastic resin layer (B), a plasticizer may be added to the resin constituting the thermoplastic resin layer (B) described above.
- plasticizer there may be used the above plasticizer which can be used in the photosensitive resin composition constituting the phosphor-containing photosensitive resin composition layer (A).
- thermoplastic resin layer (B) in the present invention can be formed into a film shape by dissolving the resin constituting the thermoplastic resin layer (B) in or mixing said resin in a solvent which dissolves said resin to prepare a uniform solution and coating the solution on the above support film by using a known coating method such as a knife coating method, a roll coating method, a spray coating method, a gravure coating method, a bar coating method and a curtain coating method, followed by drying.
- a known coating method such as a knife coating method, a roll coating method, a spray coating method, a gravure coating method, a bar coating method and a curtain coating method, followed by drying.
- the solvent which dissolves the resin constituting the thermoplastic resin layer (B) there may be mentioned, for example, water, toluene, acetone, methyl ethyl ketone, methyl isobutyl ketone, methyl cellosolve, ethyl cellosolve, ⁇ -butyrolactone, N-methylpyrrolidone, dimethylformamide, tetramethylsulfone, diethylene glycol dimethyl ether, diethylene glycol monobutyl ether, chloroform, methylene chloride, methyl alcohol and ethyl alcohol.
- solvents are used singly or in combination of two or more of them.
- the support film there may be mentioned a support film which is chemically and thermally stable and constituted by a flexible substance, for example, polyethylene terephthalate, polycarbonate, polyethylene and polypropylene. Among them, polyethylene terephthalate and polyethylene are preferred, and polyethylene terephthalate is more preferred.
- the support film can be removed later from the thermoplastic resin layer (B) so that it should not be a film subjected to surface treatment or comprising a material which makes removing impossible.
- the thickness of the support film is preferably 5 to 100 ⁇ m, more preferably 10 to 90 ⁇ m.
- a coating method a known method may be used, and there may be mentioned, for example, a knife coating method, a roll coating method, a spray coating method, a gravure coating method, a bar coating method and a curtain coating method.
- the drying temperature is preferably 60 to 130 °C, and the drying time is preferably 3 minutes to 1 hour.
- the thickness of the thermoplastic resin layer (B) in the present invention is not particularly limited, but it is preferably 10 to 200 ⁇ m, more preferably 15 to 150 ⁇ m, particularly preferably 20 to 100 ⁇ m. If the thickness is less than 10 ⁇ m, a phosphor pattern after calcination described below tends to be thin to lower light emission efficiency, while if it exceeds 200 ⁇ m, a phosphor pattern after calcination tends to be thick to reduce a light emission area of a phosphor surface, which results in lowering of light emission efficiency.
- the viscosity at 100 °C of the thermoplastic resin layer (B) in the present invention is preferably 1 to 1 x 10 9 Pa ⁇ sec, more preferably 2 to 1 x 10 8 Pa ⁇ sec, particularly preferably 5 to 1 x 10 7 Pa ⁇ sec, extremely preferably 10 to 1 x 10 6 Pa ⁇ sec. If the viscosity at 100 °C is less than 1 Pa ⁇ sec, the viscosity at room temperature becomes too low so that when a photosensitive element is prepared, the thermoplastic resin layer (B) tends to be exuded from an edge portion by flowing, and film-forming property tends to be lowered.
- thermoplastic resin layer (B) in the present invention a peelable cover film may be further laminated.
- cover film there may be mentioned polyethylene, polypropylene, polyethylene terephthalate and polycarbonate. It is preferred that the adhesive strength of the cover film to the thermoplastic resin layer (B) is smaller than the adhesive strength of the cover film to the support film.
- the thickness of the cover film is not particularly limited, but it is preferably 5 to 100 ⁇ m, more preferably 10 to 90 ⁇ m.
- the photosensitive element of the present invention obtained as described above can be stored by being wound in a roll state.
- Fig. 4 Fig. 5, Fig. 6, Fig. 7, Fig. 8, Fig. 9, Fig. 10, Fig. 11, Fig. 12 and Fig. 13.
- Fig. 4, Fig. 5, Fig. 6, Fig. 7, Fig. 8, Fig. 9, Fig. 10, Fig. 11, Fig. 12 and Fig. 13 are schematical views showing the respective steps of the processes for preparing a phosphor pattern of the present invention.
- thermoplastic resin layer (B) Step of heating and pressurizing the thermoplastic resin layer (B) in a state that the thermoplastic resin layer (B) is superposed on the phosphor-containing photosensitive resin composition layer (A) on an uneven surface of a substrate having unevenness, to laminate the phosphor-containing photosensitive resin composition layer (A) and the thermoplastic resin layer (B) on the uneven surface>
- Fig. 4 (a) shows a state that a phosphor-containing photosensitive resin composition layer (A) 7 is laminated on a substrate 1 for PDP on which a barrier rib 2 is formed.
- a lamination method for laminating the phosphor-containing photosensitive resin composition layer (A) 7 on the substrate 1 for PDP on which the barrier rib 2 is formed there may be mentioned, for example, a lamination method by using the photosensitive element constituted by the phosphor-containing photosensitive resin composition layer (A) described above.
- the photosensitive element when a cover film exists on the photosensitive element, after the cover film is removed, the photosensitive element can be laminated by contact bonding using a contact bonding roll or the like so that the phosphor-containing photosensitive resin composition layer (A) 7 is contacted with the surface on which the barrier rib is formed, of the substrate for PDP.
- the contact bonding pressure when pressurization is carried out is preferably 50 to 1 x 10 5 N/m, more preferably 2.5 x 10 2 to 5 x 10 4 N/m, particularly preferably 5 x 10 2 to 4 x 10 4 N/m in terms of line pressure. If the contact bonding pressure is less than 50 N/m, property of embedding the phosphor-containing photosensitive resin composition layer (A) 7 in the space of a concave portion of the substrate for PDP tends to be lowered, while if it exceeds 1 x 10 5 N/m, the barrier rib on the substrate for PDP tends to be broken.
- a method for making the line pressure 5 x 10 3 N/m there may be mentioned, for example, a method for making the line pressure 5 x 10 3 N/m by using a laminator having a cylinder diameter of 40 mm, using a substrate having a thickness of 3 mm, a length of 10 cm and a width of 10 cm (a square) and making the cylinder pressure (ordinary pressure 1 atm is 0) of the laminator 2 kgf/cm 2 , and a method for making the line pressure 5 x 10 3 N/m by using a laminator having a cylinder diameter of 40 mm, using a substrate having a thickness of 3 mm, a length of 20 cm and a width of 20 cm (a square) and making the cylinder pressure (ordinary pressure 1 atm is 0) of the laminator 4 kgf/cm 2 .
- the above contact bonding roll having a surface made of a material abundant in flexibility, such as rubber and plastics may be used.
- the thickness of the layer of the material abundant in flexibility is preferably 200 to 400 ⁇ m.
- lamination may be carried out by contact bonding the photosensitive element to the surface on which the barrier rib 2 is formed, of the substrate 1 for PDP while heating the photosensitive element by a heating roll 9 or the like.
- the heating temperature at the time of contact bonding under heating is preferably 10 to 140 °C, more preferably 20 to 135 °C, particularly preferably 30 to 130 °C. If the heating temperature is lower than 10 °C, the phosphor-containing photosensitive resin composition layer (A) 7 tends not to be adhered to the substrate for PDP sufficiently, while if it exceeds 140 °C, the phosphor-containing photosensitive resin composition layer (A) 7 tends to be thermoset.
- the contact bonding pressure at the time of contact bonding under heating is preferably 50 to 1 x 10 5 N/m, more preferably 2.5 x 10 2 to 5 x 10 4 N/m, particularly preferably 5 x 10 2 to 4 x 10 4 N/m in terms of line pressure. If the contact bonding pressure is less than 50 N/m, property of embedding the phosphor-containing photosensitive resin composition layer (A) 7 in the space of the concave portion of the substrate for PDP tends to be lowered, while if it exceeds 1 x 10 5 N/m, the barrier rib on the substrate for PDP tends to be broken.
- the preheating temperature is preferably 30 to 130 °C, and the preheating time is preferably 0.5 to 20 minutes.
- operations of the above contact bonding and contact bonding under heating may be carried out under a reduced pressure of 5 x 10 4 Pa or less.
- heating may be carried out at a temperature range of 30 to 150 °C for 1 to 120 minutes. At the time of heating, a support film may be removed, if necessary.
- the phosphor-containing photosensitive resin composition layer (A) 7 can be laminated on the substrate 1 for PDP on which the barrier rib 2 is formed.
- Fig. 4 (b) shows a state that a thermoplastic resin layer (B) 8 is superposed on the phosphor-containing photosensitive resin composition layer (A) 7, and the phosphor-containing photosensitive resin composition layer (A) 7 and the thermoplastic resin layer (B) 8 are laminated while carrying out contact bonding under heating.
- thermoplastic resin layer (B) 8 As a method for superposing the thermoplastic resin layer (B) 8 on the phosphor-containing photosensitive resin composition layer (A) 7 and carrying out contact bonding under heating, there may be mentioned, for example, a method in which when a support film exists on the phosphor-containing photosensitive resin composition layer (A) 7 in the state of Fig. 4 (a), after the support film is removed, (when a cover film exists on the thermoplastic resin layer (B) 8, after the cover film is removed), the thermoplastic resin layer (B) 8 is superposed on the phosphor-containing photosensitive resin composition layer (A) 7, and contact bonding under heating is carried out by the heating roll 9 or the like.
- the heating temperature at the time of contact bonding under heating is preferably 10 to 140 °C, more preferably 20 to 135 °C, particularly preferably 30 to 130 °C. If the heating temperature is lower than 10 °C, property of embedding the phosphor-containing photosensitive resin composition layer (A) 7 in the space of the substrate for PDP tends to be lowered, while if it exceeds 140 °C, the phosphor-containing photosensitive resin composition layer (A) 7 tends to be thermoset.
- the contact bonding pressure at the time of contact bonding under heating is preferably 50 to 1 x 10 5 N/m, more preferably 2.5 x 10 2 to 5 x 10 4 N/m, particularly preferably 5 x 10 2 to 4 x 10 4 N/m in terms of line pressure. If the contact bonding pressure is less than 50 N/m, property of embedding the phosphor-containing photosensitive resin composition layer (A) 7 in the space of the concave portion of the substrate for PDP tends to be lowered, while if it exceeds 1 x 10 5 N/m, the barrier rib on the substrate for PDP tends to be broken.
- thermoplastic resin layer (B) 8 When the thermoplastic resin layer (B) 8 is heated as described above, it is not necessary to carry out preheat treatment of the substrate for PDP on which the phosphor-containing photosensitive resin composition layer (A) 7 is laminated. However, from the point that property of embedding the phosphor-containing photosensitive resin composition layer (A) 7 in the space of the concave portion is further improved, it is preferred to carry out preheat treatment of the substrate for PDP on which the phosphor-containing photosensitive resin composition layer (A) 7 is laminated.
- the preheating temperature is preferably 30 to 130 °C, and the preheating time is preferably 0.5 to 20 minutes.
- the above heating roll 9 having a surface made of a material abundant in flexibility, such as rubber and plastics may be used.
- the thickness of the layer of the material abundant in flexibility is preferably 200 to 400 ⁇ m.
- operations of the above contact bonding and contact bonding under heating may be carried out under a reduced pressure of 5 x 10 4 Pa or less.
- heating may be carried out at a temperature range of 30 to 150 °C for 1 to 120 minutes.
- the support film may be removed, if necessary.
- the phosphor-containing photosensitive resin composition layer (A) 7 can be formed uniformly in the space of the concave portion of the substrate 1 for PDP.
- both of the phosphor-containing photosensitive resin composition layer (A) 7 and the thermoplastic resin layer (B) 8 may be laminated simultaneously which carrying out contact bonding under heating.
- thermoplastic resin layer (B) 8 As conditions of contact bonding under heating when contact bonding under heating of both of the layers is carried out simultaneously, there may be used the above conditions under which contact bonding under heating of the thermoplastic resin layer (B) 8 is carried out.
- Fig. 6 is one embodiment after completion of the step of Fig. 4 (b) in the process for preparing a phosphor pattern of the present invention.
- the layer thicknesses of the phosphor-containing photosensitive resin composition layer (A) 7 and the thermoplastic resin layer (B) 8 from the point that a phosphor pattern with high precision and a uniform shape can be formed, it is preferred that in the phosphor-containing photosensitive resin composition layer (A) and the thermoplastic resin layer (B) in a region which is the same as the region where unevenness is formed on a substrate having unevenness (a substrate for PDP), the ratio (V 1 )/(V 2 ) of the total volume (V 1 ) of the phosphor-containing photosensitive resin composition layer (A) and the thermoplastic resin layer (B) to the volume (V 2 ) of the space of a concave portion of the substrate having unevenness is in the range of 1 to 2.
- the phosphor-containing photosensitive resin composition layer (A) 7 tends to be formed on the inner surface of the concave portion in a state that almost none of the phosphor-containing photosensitive resin composition layer (A) 7 remains on the convex portion as shown in Fig. 4 (b). If (V 1 )/(V 2 ) exceeds 1.05 and is 2 or less, the phosphor-containing photosensitive resin composition layer (A) 7 tends to be formed on the inner surface of the concave portion in a state that the phosphor-containing photosensitive resin composition layer (A) 7 remains on the convex portion as shown in Fig. 6.
- the phosphor-containing photosensitive resin composition layer (A) 7 is laminated on the inner surface (the wall surface of the barrier rib 2 and the surface of the substrate 1) of the concave portion so that almost none of the phosphor-containing photosensitive resin composition layer (A) 7 remains on the convex portion (the barrier rib 2) as shown in Fig. 4 (b).
- lamination may be carried out as shown in Fig. 4 (b), or lamination may be carried out in a state that the phosphor-containing photosensitive resin composition layer (A) 7 remains on the convex portion as shown in Fig. 6.
- the phosphor-containing photosensitive resin composition layer (A) 7 can be laminated uniformly on the surface (on the uneven surface) of the substrate 1 for PDP on which the barrier rib 2 is formed.
- Fig. 4 (c) shows a state that active light 11 is irradiated imagewisely.
- a method for irradiating the active light 11 imagewisely there may be used a method of irradiating the active light 11 imagewisely through a photomask 10 such as a negative film and a positive film, provided above the thermoplastic resin layer (B) 8 in the state of Fig. 4 (b).
- a photomask 10 such as a negative film and a positive film
- the active light 11 may be irradiated imagewisely while the support film is laminated as such, or the active light 11 may be irradiated imagewisely after the support film is removed.
- thermoplastic resin layer (B) 8 is the photosensitive resin composition described above, the phosphor-containing photosensitive resin composition layer (A) 7 and the thermoplastic resin layer (B) 8 are to be photocured simultaneously.
- the permeation width of the active light 11 of the photomask 10 is the same permeation width as the opening width of the concave portion of the substrate for PDP or wider than the opening width of the concave portion of the substrate for PDP.
- photomask 10 has an active light permeation width which is narrower than the opening width of the concave portion.
- the active light permeation width which is narrower than the opening width of the concave portion is preferably 0.3 x W to 0.99999 x W, more preferably 0.5 x W to 0.999 x W, particularly preferably 0.6 x W to 0.99 x W.
- the active light permeation width which is narrower than the opening width of the concave portion is less than 0.3 x W, photocuring of the phosphor-containing photosensitive resin composition layer (A) 7 formed on the inner surface of the concave portion tends to be insufficient.
- developing solution resistance (property that a portion which remains without being removed by development and becomes a pattern is not corroded by development) of the phosphor-containing photosensitive resin composition layer (A) 7 formed on the inner surface of the concave portion tends to be lowered, and even a necessary portion of the phosphor-containing photosensitive resin composition layer (A) 7 formed on the inner surface of the concave portion tends to be removed.
- the active light permeation width which is narrower than the opening width of the concave portion is a width exceeding 0.99999 x W, even a portion other than the inner surface of the concave portion to be photocured tends to be photocured, and an unnecessary portion tends to remain after development described below.
- the active light may be irradiated imagewisely in a state that a gas containing oxygen exists on the thermoplastic resin layer (B) 8.
- the photopolymerization initiator (c) which produces free radical by irradiation of active light in the photosensitive resin composition constituting the phosphor-containing photosensitive resin composition layer (A) 7 is a photopolymerization initiator in which free radical is produced by irradiation of active light and produced free radical is easily deactivated by oxygen.
- thermoplastic resin layer (B) 8 may be the photosensitive resin composition described above, and it is preferred that the photopolymerization initiator (j) which produces free radical by irradiation of active light, constituting the thermoplastic resin layer (B) 8 is a photopolymerization initiator in which free radical is produced by irradiation of active light and produced free radical is easily deactivated by oxygen.
- Fig. 7 shows a state that the active light 11 is irradiated imagewisely in a state that a gas containing oxygen exists on the thermoplastic resin layer (B) 8.
- thermoplastic resin layer (B) 8 it is necessary to irradiate the active light 11 imagewisely in a state that a gas containing oxygen always exists on the thermoplastic resin layer (B) 8.
- a method for such irradiation there may be mentioned, for example, a method in which the active light 11 is irradiated imagewisely in a state that the thermoplastic resin layer (B) 8 is directly contacted with air or the like, through the photomask 10 such as a negative film, a negative glass, a positive film and a positive glass with a spacer 12 or the like being sandwiched between the thermoplastic resin layer (B) 8 and the photomask 10.
- the active light 11 can be also irradiated imagewisely in a state that the photomask 10 is directly superposed on the thermoplastic resin layer (B) 8 without sandwiching the spacer 12 or the like between the thermoplastic resin layer (B) 8 and the photomask 10.
- thermoplastic resin layer (B) 8 when a support film exists on the thermoplastic resin layer (B) 8, if a portion to be exposed of the phosphor-containing photosensitive resin composition layer (A) 7 formed on a portion other than the inner surface of the concave portion and the thermoplastic resin layer (B) 8 are a photosensitive resin composition, in order that the photocuring property of a portion to be exposed of the thermoplastic resin layer (B) 8 is made insufficient by oxygen and an unnecessary portion thereof is removed by development described below, it is necessary to irradiate the active light 11 imagewisely after the support film is removed. However, when the support film is a film having oxygen permeability, the active light 11 can be irradiated imagewisely in a state that the support film is laminated.
- a portion to be exposed of the phosphor-containing photosensitive resin composition layer (A) 7 formed on a portion other than the inner surface of the concave portion and the thermoplastic resin layer (B) 8 are a photosensitive resin composition
- the photocured thermoplastic resin layer (B) 8 is formed on the inner surface of the concave portion.
- the thermoplastic resin layer (B) 8 having insufficient photocuring property is formed on a portion other than the inner surface of the concave portion.
- the active light 11 may be irradiated imagewisely through the photomask 10 such as a negative film and a positive film.
- the active light 11 a known active light source may be used, and there may be mentioned, for example, light generated from carbon arc, mercury vapor arc, xenon arc or the like.
- the sensitivity of a photopolymerization initiator is generally the largest in a UV ray region so that in that case, an active light source which radiates UV ray effectively should be used.
- an active light source which radiates UV ray effectively should be used.
- the photopolymerization initiator is sensitive to visible rays, for example, it is 9,10-phenanthrenequinone, visible light can be used as the active light 11, and as a light source thereof, there may be also used, in addition to the above light sources, a flood bulb for photographs and a solar lamp.
- parallel light non-parallel light and scattered light.
- parallel light non-parallel light or scattered light
- one or two or all of them may be used in one step, and two of them may be used in two stages or all of them may be used in all stages separately.
- two of them are used in two stages or all of them are used in all stages separately, either of them may be used firstly.
- the irradiation dose of the active light 11 is preferably 3 mJ/cm 2 to 3 J/cm 2 , more preferably 5 mJ/cm 2 to 1 J/cm 2 , particularly preferably 10 mJ/cm 2 to 1 J/cm 2 .
- active light can be irradiated imagewisely with high precision and good operatability.
- Fig. 5 (a) shows a state that unnecessary portions are removed by development.
- 7' is a phosphor-containing photosensitive resin composition layer after photocuring.
- a development method there may be mentioned, for example, a method in which after the state of Fig. 4 (c), when a support film exists on the thermoplastic resin layer (B) 8, after the support film is removed, development is carried out by using a known developing solution such as water, an alkaline aqueous solution, an aqueous developing solution (which comprises water and at least one organic solvent or an alkaline aqueous solution and at least one organic solvent) and an organic solvent according to a known method such as spraying, dipping by rocking, blushing and scrapping to remove unnecessary portions.
- a known developing solution such as water, an alkaline aqueous solution, an aqueous developing solution (which comprises water and at least one organic solvent or an alkaline aqueous solution and at least one organic solvent) and an organic solvent according to a known method such as spraying, dipping by rocking, blushing and scrapping to remove unnecessary portions.
- the thermoplastic resin layer (B) 8 is removed by dissolution using water, an alkaline aqueous solution, an aqueous developing solution, an organic solvent or the like which does not dissolve the phosphor-containing photosensitive resin composition layer (A) 7, and then the unnecessary portion of the phosphor-containing photosensitive resin composition layer (A) 7 may be removed by using a developing solution. Also, when the phosphor-containing photosensitive resin composition layer (A) 7 and the thermoplastic resin layer (B) 8 can be developed by using the same developing solution, the unnecessary portion of the phosphor-containing photosensitive resin composition layer (A) 7 and the thermoplastic resin layer (B) 8 can be removed in one step by using such a developing solution.
- thermoplastic resin layer (B) 8 is the photosensitive resin composition described above, a thermoplastic resin layer (B) 8' after photocuring remains on the phosphor-containing photosensitive resin composition layer (A) 7' after photocuring.
- Fig. 8 shows a state that the thermoplastic resin layer (B) 8' after photocuring remains on the phosphor-containing photosensitive resin composition layer (A) 7' after photocuring.
- the developing time and the developing temperature can be adjusted suitably so that the unnecessary portions are removed.
- the developing time is preferably 1 to 10 times the shortest developing time of the phosphor-containing photosensitive resin composition layer (A) 7 (the shortest time until the phosphor-containing photosensitive resin composition layer (A) is removed by development after the layer (A) is embedded in the inner surface of the concave portion of the substrate for PDP), and the developing temperature is preferably 10 to 60 °C.
- the developing time is shorter than the shortest developing time, an undeveloped portion tends to be generated, while if it exceeds 10 times the shortest developing time, even a necessary portion of the phosphor-containing photosensitive resin composition layer (A) 7 tends to be removed. If the developing temperature is lower than 10 °C, developability tends to be lowered, while if it exceeds 60 °C, developing solution resistance tends to be lowered.
- an alkali hydroxide e.g., a hydroxide of lithium, sodium or potassium
- an alkali carbonate e.g., a carbonate or bicarbonate of lithium, sodium or potassium
- an alkali metal phosphate e.g., potassium phosphate and sodium phosphate
- an alkali metal pyrophosphate e.g., sodium pyrophosphate and potassium pyrophosphate
- sodium carbonate and tetramethylammonium hydroxide are preferred.
- the pH of the alkaline aqueous solution to be used for development is preferably 9 to 11.
- the temperature can be adjusted depending on the developabilities of the phosphor-containing photosensitive resin composition layer (A) 7 and the thermoplastic resin layer (B) 8.
- a surfactant In the alkaline aqueous solution, a surfactant, a defoaming agent and a small amount of an organic solvent for accelerating development may be mixed.
- aqueous developing solution there may be mentioned an aqueous developing solution comprising water and at least one organic solvent or an alkaline aqueous solution and at least one organic solvent.
- aqueous developing solution comprising water and at least one organic solvent
- the organic solvent there may be mentioned, for example, acetone alcohol, acetone, ethyl acetate, an alkoxyethanol having an alkoxy group with 1 to 4 carbon atoms, ethyl alcohol, isopropyl alcohol, butyl alcohol, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, diethylene glycol monobutyl ether, triethylene glycol monobutyl ether,.dipropylene glycol monomethyl ether, dipropylene glycol monopropyl ether, 3-methyl-3-methoxybutyl acetate, 1,1,1-trichloroethane, N-methylpyrrolidone, N,N-dimethylformamide, cyclohexanone, methyl isobutyl ketone and ⁇ -butyrolactone.
- organic solvents are used singly or in combination of two or more of them.
- the concentration of the organic solvent is generally in the range of 2 to 95 % by weight, and the temperature can be adjusted depending on developability.
- aqueous developing solution comprising an alkaline aqueous solution and at least one organic solvent, as a base of the alkaline aqueous solution
- organic solvent for example, borax, sodium metasilicate, ethanolamine, ethylenediamine, diethylenetriamine, 2-amino-2-hydroxymethyl-1,3-propanediol, 1,3-diaminopropanol-2-morpholine and tetramethylammonium hydroxide in addition to the above compounds.
- the pH of the aqueous developing solution comprising an alkaline aqueous solution and at least one organic solvent is preferably 8 to 12, more preferably 9 to 10.
- organic solvent of the aqueous developing solution comprising an alkaline aqueous solution and at least one organic solvent
- organic solvent there may be mentioned, for example, acetone alcohol, acetone, ethyl acetate, an alkoxyethanol having an alkoxy group with 1 to 4 carbon atoms, ethyl alcohol, isopropyl alcohol, butyl alcohol, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether and diethylene glycol monobutyl ether.
- organic solvents are used singly or in combination of two or more of them.
- the concentration of the organic solvent is generally in the range of 2 to 95 % by weight, and the temperature can be adjusted depending on developability.
- a surfactant and a defoaming agent may be mixed.
- organic solvent to be used singly as a developing solution there may be mentioned, for example, acetone alcohol, acetone, ethyl acetate, an alkoxyethanol having an alkoxy group with 1 to 4 carbon atoms, ethyl alcohol, isopropyl alcohol, butyl alcohol, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, diethylene glycol monobutyl ether, triethylene glycol monobutyl ether, dipropylene glycol monomethyl ether, dipropylene glycol monopropyl ether, 3-methyl-3-methoxybutyl acetate, 1,1,1-trichloroethane, N-methylpyrrolidone, N,N-dimethylformamide, cyclohexanone, methyl isobutyl ketone and ⁇ -butyrolactone.
- water in the range of 1 to 20 % by weight may be added to these organic solvents.
- an alkali metal ion or a metal ion is not contained in a known developing solution such as water, an alkaline solution, an aqueous developing solution (which comprises water and at least one organic solvent or an alkaline aqueous solution and at least one organic solvent) and an organic solvent.
- a known developing solution such as water, an alkaline solution, an aqueous developing solution (which comprises water and at least one organic solvent or an alkaline aqueous solution and at least one organic solvent) and an organic solvent.
- the base of the alkaline aqueous solution remaining on the phosphor-containing photosensitive resin composition layer (A) 7' after photocuring may be subjected to acid treatment (neutralization treatment) by using an organic acid, an inorganic acid or an acid aqueous solution thereof according to a known method such as spraying, dipping by rocking, blushing and scrapping.
- an organic acid and an inorganic acid such as a saturated aliphatic acid, an unsaturated aliphatic acid, an aliphatic dibasic acid, an aromatic dibasic acid, an aliphatic tribasic acid and an aromatic tribasic acid.
- organic acid there may be mentioned, for example, formic acid, acetic acid, chloroacetic acid, dichloroacetic acid, trichloroacetic acid, propionic acid capric acid, undecanoic acid, lauric acid, tridecanoic acid, myristic acid, pentadecanoic acid, palmitic acid, heptadecanoic acid, stearic acid, nonadecanoic acid, arachidic acid, palmitoleic acid, oleic acid, elaidic acid, linolenic acid, linoleic acid, oxalic acid, malonic acid, methylmalonic acid, ethylmalonic acid, monomethyl malonate, monoethyl malonate, succinic acid, methylsuccinic acid, adipic acid, methyladipic acid, pimelic acid, suberic acid, azelaic acid, sebacic acid, maleic acid, itaconic acid,
- inorganic acid there may be mentioned, for example, sulfuric acid, hydrochloric acid and nitric acid.
- the pH of the acid aqueous solution to be used for acid treatment is preferably 2 to 6, and the pH and temperature of the acid aqueous solution can be adjusted depending on acid resistances (durabilities that deterioration is not caused by acid) of the phosphor-containing photosensitive resin composition layer (A) 7' after photocuring and the substrate 1 for PDP (the substrate having unevenness).
- a step of water washing may be carried out.
- the respective removals may be carried out separately by dry development in which only an unnecessary portion having adhesiveness of the phosphor-containing photosensitive resin composition layer (A) 7 is peeled off by utilizing difference in adhesiveness between an exposed portion and an unexposed portion, or may be carried out in one step.
- irradiation of UV ray by a high pressure mercury lamp or the like and heating may be also carried out.
- the irradiation dose of UV ray is not particularly limited, but from the point of photocuring property, it is preferably 5 to 10,000 mJ/cm 2 , more preferably 7 to 5,000 mJ/cm 2 , particularly preferably 10 to 3,000 mJ/cm 2 .
- the temperature at the time of heating is preferably 60 to 180 °C, more preferably 100 to 180 °C.
- the heating time is preferably 15 to 90 minutes.
- UV ray and heating may be carried out separately, and either of them may be carried out previously.
- the step (IIIa) As described above, by carrying out this step (the step (IIIa)), the phosphor-containing photosensitive resin composition layer after photocuring, from which the unnecessary portion is removed is formed.
- a state shown in Fig. 9 tends to occur depending on the exposure and development conditions and positional displacement of the photomask.
- thermoplastic resin layer (B) 8 is a photosensitive resin composition
- a state shown in Fig. 10 tends to occur from the same reason.
- thermoplastic resin layer (the unnecessary portion) after photocuring when the phosphor-containing photosensitive resin composition layer (the unnecessary portion) after photocuring, which remains on a portion other than the inner surface of the concave portion and the thermoplastic resin layer (B) 8 is a photosensitive resin composition, the thermoplastic resin layer (the unnecessary portion) after photocuring may be removed completely by polishing or the like.
- Fig. 9 is a schematical view showing a state of the case where after this step (the step (IIIa)) is carried out, the phosphor-containing photosensitive resin composition layer (A) 7' after photocuring remains on a portion other than the inner surface of the concave portion.
- Fig. 9, 13 is an unnecessary portion (a portion to be removed completely by polishing or the like).
- Fig. 10 shows a schematical view of the same case in which the thermoplastic resin layer (B) 8' after photocuring is a photosensitive resin composition.
- only the unnecessary portion 13 can be also removed physically by adhering an adhesive tape to the unnecessary portion 13 and then peeling the adhesive tape in place of carrying out polishing as described above.
- a black inorganic material paste containing a black inorganic pigment such as iron oxide, chromium oxide and copper oxide and a low melting point glass frit or the like is coated or printed on the convex portion, or black strips are formed by using a black inorganic material-containing photosensitive element, and then calcination described below can be carried out.
- the phosphor-containing photosensitive resin composition layer (A) 7' after photocuring can be formed on the inner surface (the wall surface of the barrier rib 2 and the surface of the substrate 1) of the concave portion of the substrate having unevenness (the substrate for PDP) with a good shape and good operatability.
- Fig. 5 (b) shows a state that a phosphor pattern after removing unnecessary components by calcination is formed is shown.
- 5 is a phosphor pattern.
- a calcination method is not particularly limited, and the phosphor pattern 5 can be formed by removing unnecessary components other than the phosphor and the binding agent according to a known calcination method.
- the temperature-elevating rate at the time of calcination is preferably 0.5 to 50 °C/min, more preferably 1 to 45 °C/min.
- the highest calcination temperature is preferably 350 to 800 °C, more preferably 400 to 600 °C.
- the calcination time at the highest calcination temperature is preferably 3 to 120 minutes, more preferably 5 to 90 minutes.
- a step of maintaining that temperature may be provided, and the maintaining time is preferably 5 to 100 minutes.
- the phosphor pattern 5 can be formed on the inner surface (the wall surface of the barrier rib 2 and the surface of the substrate 1) of the concave portion of the substrate having unevenness (the substrate for PDP) with a good shape and good operatability.
- a multicolor pattern comprising photosensitive resin composition layers each containing a phosphor which emits red, green or blue light is formed by repeating the respective steps of (Ia) to (IIIa) of the above process of the present invention for every color, the step of (IVa) is carried out to form a multicolor phosphor pattern.
- pattern formations of red, blue and green may be carried out in any order.
- Fig. 11 shows a state that a multicolor pattern comprising photosensitive resin composition layers each containing a phosphor which emits red, green or blue light is formed by repeating the respective steps (Ia) to (IIIa) in the present invention for every color.
- 7'a is a pattern of a first color
- 7'b is a pattern of a second color
- 7'c is a pattern of a third color.
- Fig. 12 shows a state that in the case where the thermoplastic resin layer (B) 8 is a photosensitive resin composition, a multicolor pattern comprising photosensitive resin composition layers each containing a phosphor which emits red, green or blue light is formed by repeating the respective steps (Ia) to (IIIa) in the present invention for every color.
- Fig. 13 shows a state that a multicolor phosphor pattern is formed by carrying out the step of (IVa) in the present invention.
- 5a is a phosphor pattern of a first color
- 5b is a phosphor pattern of a second color
- 5c is a phosphor pattern of a third color.
- a multicolor phosphor pattern which emit red, green and blue lights is formed by repeating the respective steps of (Ia) to (IVa) in the above process of the present invention for every color.
- a multicolor phosphor pattern can be formed on the inner surface (the wall surface of the barrier rib 2 and the surface of the substrate 1) of the concave portion of the substrate having unevenness (the substrate for PDP) with a good shape and good operatability.
- the photosensitive element in the present invention has a support film, the thermoplastic resin layer (B) on the support film and the phosphor-containing photosensitive resin composition layer (A) thereon.
- the photosensitive element in the present invention can be obtained by dissolving the above resin constituting the thermoplastic resin layer (B) in or mixing said resin with a solvent which dissolves said resin to prepare a uniform solution, coating the solution on the above support film by using a known coating method such as a knife coating method, a roll coating method, a spray coating method, a gravure coating method, a bar coating method and a curtain coating method, followed by drying, dissolving the above respective components constituting the phosphor-containing photosensitive resin composition layer (A) in or mixing said components with a solvent which can dissolve or disperse said components to prepare a solution in which said components are dispersed uniformly and coating the solution on the thermoplastic resin layer (B) provided as described above by using a known coating method such as a knife coating method, a roll coating method, a spray coating method, a gravure coating method, a bar coating method and a curtain coating method, followed by drying.
- a known coating method such as a knife coating method, a roll coating method, a spray
- the solvent which dissolves the resin constituting the thermoplastic resin layer (B) and the above respective components constituting the phosphor-containing photosensitive resin composition layer (A) there may be mentioned, for example, water, toluene, acetone, methyl ethyl ketone, methyl isobutyl ketone, methyl cellosolve, ethyl cellosolve, ⁇ -butyrolactone, N-methylpyrrolidone, dimethylformamide, tetramethylsulfone, diethylene glycol dimethyl ether, diethylene glycol monobutyl ether, chloroform, methylene chloride, methyl alcohol and ethyl alcohol.
- solvents are used singly or in combination of two or more of them.
- the material of a portion of a coating apparatus, contacted with the solution in which the above respective components constituting the phosphor-containing photosensitive resin composition layer (A) are dispersed uniformly by dissolving said components in or mixing said components with the solvent which can dissolve or disperse said components is preferably a non-metallic material.
- the coating apparatus contacted with the solution constituting the phosphor-containing photosensitive resin composition layer (A) is polished by the phosphor in said solution, and powder generated by polishing tends to migrate, as impurity, into the solution constituting the phosphor-containing photosensitive resin composition layer (A).
- the drying temperature is preferably 60 to 130 °C, and the drying time is preferably 3 minutes to 1 hour.
- the thickness of the phosphor-containing photosensitive resin composition layer (A) in the present invention is not particularly limited, but it is preferably 10 to 200 ⁇ m, more preferably 15 to 150 ⁇ m, particularly preferably 20 to 100 ⁇ m. If the thickness is less than 10 ⁇ m, a phosphor pattern after calcination described below tends to be thin to lower light emission efficiency, while if it exceeds 200 ⁇ m, a phosphor pattern after calcination tends to be thick to reduce a light emission area of a phosphor surface, which results in lowering of light emission efficiency.
- the thickness of the thermoplastic resin layer (B) in the present invention is not particularly limited, but it is preferably 10 to 200 ⁇ m, more preferably 15 to 150 ⁇ m, particularly preferably 20 to 100 ⁇ m. If the thickness is less than 10 ⁇ m, a phosphor pattern after calcination described below tends to be thin to lower light emission efficiency, while if it exceeds 200 ⁇ m, a phosphor pattern after calcination tends to be thick to reduce a light emission area of a phosphor surface, which results in lowering of light emission efficiency.
- the above peelable cover film may be further laminated.
- the cover film there may be mentioned polyethylene, polypropylene, polyethylene terephthalate and polycarbonate. It is preferred that the adhesive strength of the cover film to the phosphor-containing photosensitive resin composition layer (A) is smaller than the adhesive strength of the support film to the thermoplastic resin layer (B) and the adhesive strength of the thermoplastic resin layer (B) to the phosphor-containing photosensitive resin composition layer (A).
- the photosensitive element of the present invention can be also obtained by coating the solution in which the above respective components constituting the phosphor-containing photosensitive resin composition layer (A) are dispersed uniformly obtained by dissolving said components in or mixing said components with the above solvent which can dissolve or disperse said components, on the above support film by using a known coating method such as a knife coating method, a roll coating method, a spray coating method, a gravure coating method, a bar coating method and a curtain coating method, followed by drying, to form the phosphor-containing photosensitive resin composition layer (A) and then pasting the phosphor-containing photosensitive resin composition layer (A) and the thermoplastic resin layer (B) provided on the above support film so that both layers are contacted.
- a known coating method such as a knife coating method, a roll coating method, a spray coating method, a gravure coating method, a bar coating method and a curtain coating method, followed by drying, to form the phosphor-containing photosensitive resin composition layer (A) and then pasting the
- the adhesive strength of the support film with which the phosphor-containing photosensitive resin composition layer (A) is contacted to the phosphor-containing photosensitive resin composition layer (A) is smaller than the adhesive strength of the support film with which the thermoplastic resin layer (B) is contacted to the thermoplastic resin layer (B) and the adhesive strength of the thermoplastic resin layer (B) to the phosphor-containing photosensitive resin composition layer (A).
- the photosensitive element of the present invention obtained as described above can be stored by being wound in a roll state.
- the respective steps of the process for preparing a phosphor pattern of the present invention including (Ib) a step of heating and pressurizing a photosensitive element having a support film, the thermoplastic resin layer (B) provided on the support film and the phosphor-containing photosensitive resin composition layer (A) provided thereon so that the phosphor-containing photosensitive resin composition layer (A) is contacted with an uneven surface of a substrate having unevenness, to laminate the phosphor-containing photosensitive resin composition layer (A) and the thermoplastic resin layer (B) on the uneven surface; (IIb) a step of irradiating the phosphor-containing photosensitive resin composition layer (A) and/or the thermoplastic resin layer (B) imagewisely with active light; (IIIb) a step of removing unnecessary portions from the phosphor-containing photosensitive resin composition layer (A) and/or the thermoplastic resin layer (B) by development; and (IVb) a step of removing unnecessary components from the phosphor-containing photosensitive resin composition layer (A)
- ⁇ (Ib) Step of heating and pressurizing a photosensitive element having a support film, the thermoplastic resin layer (B) provided on the support film and the phosphor-containing photosensitive resin composition layer (A) provided thereon so that the phosphor-containing photosensitive resin composition layer (A) is contacted with an uneven surface of a substrate having unevenness, to laminate the phosphor-containing photosensitive resin composition layer (A) and the thermoplastic resin layer (B) on the uneven surface>
- Fig. 14 shows a state that the photosensitive element of the present invention including the thermoplastic resin layer (B) 8 and the phosphor-containing photosensitive resin composition layer (A) 7 is laminated by using a heating roll 9, on the uneven surface of the above substrate 1 for PDP (the substrate having unevenness) on which the barrier rib 2 is formed.
- a method for laminating the photosensitive element of the present invention including the thermoplastic resin layer (B) 8 and the phosphor-containing photosensitive resin composition layer (A) 7 on the substrate 1 for PDP on which the barrier rib 2 is formed there may be mentioned, for example, a method in which when a cover film exists on the photosensitive element, after the cover film is removed (when a photosensitive element obtained by pasting the thermoplastic resin layer (B) formed on a support film and the phosphor-containing photosensitive resin composition layer (A) formed on a support film is used, after the support film of the phosphor-containing photosensitive resin composition layer (A) is removed), lamination is carried out by contact bonding under heating of the photosensitive element by the heating roll 9 so that the phosphor-containing photosensitive resin composition layer (A) 7 is contacted with the surface on which the barrier rib 2 is formed, of the substrate 1 for PDP.
- the heating temperature at the time of contact bonding under heating is preferably 10 to 140 °C, more preferably 20 to 135 °C, particularly preferably 30 to 130 °C. If the heating temperature is lower than 10 °C, property of embedding the phosphor-containing photosensitive resin composition layer (A) 7 in the space of the substrate for PDP tends to be lowered, while if it exceeds 140 °C, the phosphor-containing photosensitive resin composition layer (A) 7 tends to be thermoset.
- the contact bonding pressure at the time of contact bonding under heating is preferably 50 to 1 x 10 5 N/m, more preferably 2.5 x 10 2 to 5 x 10 4 N/m, particularly preferably 5 x 10 2 to 4 x 10 4 N/m in terms of line pressure. If the contact bonding pressure is less than 50 N/m, property of embedding the phosphor-containing photosensitive resin composition layer (A) 7 in the space of the concave portion of the substrate for PDP tends to be lowered, while if it exceeds 1 x 10 5 N/m, the barrier rib on the substrate for PDP tends to be broken.
- the photosensitive element of the present invention including the thermoplastic resin layer (B) 8 and the phosphor-containing photosensitive resin composition layer (A) 7 is heated as described above, it is not necessary to carry out preheat treatment of the substrate for PDP. However, from the point that property of embedding the phosphor-containing photosensitive resin composition layer (A) 7 in the space of the concave portion is further improved, it is preferred to carry out preheat treatment of the substrate for PDP.
- the preheating temperature is preferably 30 to 140 °C, and the preheating time is preferably 0.5 to 20 minutes.
- the above heating roll 9 having a surface made of a material abundant in flexibility, such as rubber and plastics may be used.
- the thickness of the layer of the material abundant in flexibility is preferably 200 to 400 ⁇ m.
- operations of the above contact bonding and contact bonding under heating may be carried out under a reduced pressure of 5 x 10 4 Pa or less.
- heating may be carried out at a temperature range of 30 to 150 °C for 1 to 120 minutes.
- the support film may be removed, if necessary.
- the phosphor-containing photosensitive resin composition layer (A) 7 can be formed uniformly in the space of the concave portion of the substrate for PDP.
- the layers can be laminated in a state as shown in Fig. 6.
- the layer thicknesses of the phosphor-containing photosensitive resin composition layer (A) 7 and the thermoplastic resin layer (B) 8 from the point that a phosphor pattern with high precision and a uniform shape can be formed, it is preferred that in the phosphor-containing photosensitive resin composition layer (A) and the thermoplastic resin layer (B) in a region which is the same as the region where unevenness is formed on a substrate having unevenness (a substrate for PDP), the ratio (V 1 )/(V 2 ) of the total volume (V 1 ) of the phosphor-containing photosensitive resin composition layer (A) and the thermoplastic resin layer (B) to the volume (V 2 ) of the space of a concave portion of the substrate having unevenness is in the range of 1 to 2.
- the phosphor-containing photosensitive resin composition layer (A) 7 tends to be formed on the inner surface of the concave portion in a state that almost none of the phosphor-containing photosensitive resin composition layer (A) 7 remains on the convex portion as shown in Fig. 14. If (V 1 )/(V 2 ) exceeds 1.05 and is 2 or less, the phosphor-containing photosensitive resin composition layer (A) 7 tends to be formed on the inner surface of the concave portion in a state that the phosphor-containing photosensitive resin composition layer (A) 7 remains on the convex portion as shown in Fig. 6.
- the phosphor-containing photosensitive resin composition layer (A) 7 is laminated on the inner surface of the concave portion so that almost none of the phosphor-containing photosensitive resin composition layer (A) 7 remains on the convex portion as shown in Fig. 14.
- lamination may be carried out as shown in Fig. 14, or lamination may be carried out in a state that the phosphor-containing photosensitive resin composition layer (A) 7 remains on the convex portion as shown in Fig. 6.
- the phosphor-containing photosensitive resin composition layer (A) 7 can be laminated uniformly on the surface (on the uneven surface) of the substrate 1 for PDP on which the barrier rib 2 is formed.
- thermoplastic resin layer (B) As a method for irradiating the phosphor-containing photosensitive resin composition layer (A) and/or the thermoplastic resin layer (B) imagewisely with active light, there may be used all of the same methods as in the above step (IIa) of irradiating the phosphor-containing photosensitive resin composition layer (A) and/or the thermoplastic resin layer (B) imagewisely with active light.
- thermoplastic resin layer (B) As a method for removing unnecessary portions from the phosphor-containing photosensitive resin composition layer (A) and/or the thermoplastic resin layer (B) by development, there may be used all of the same methods as in the above step (IIIa) of removing unnecessary portions from the phosphor-containing photosensitive resin composition layer (A) and/or the thermoplastic resin layer (B) by development.
- thermoplastic resin layer (B) As a method for removing unnecessary components from the phosphor-containing photosensitive resin composition layer (A) and/or the thermoplastic resin layer (B) by calcination, there may be used all of the same methods as in the above step (IVa) of removing unnecessary components from the phosphor-containing photosensitive resin composition layer (A) and/or the thermoplastic resin layer (B) by calcination.
- a multicolor pattern comprising photosensitive resin composition layers each containing a phosphor which emits red, green or blue light is formed by repeating the respective steps of (Ib) to (IIIb) of the above process of the present invention for every color, the step of (IVb) is carried out to form a multicolor phosphor pattern.
- pattern formations of red, blue and green may be carried out in any order.
- a multicolor phosphor pattern which emit red, green and blue lights is formed by repeating the respective steps of (Ib) to (IVb) in the above process of the present invention for every color.
- a material constituting the embedding layer (C) in the present invention is not particularly limited so long as it is deformed by stress from the outside and can be peeled off from the phosphor-containing photosensitive resin composition layer (A).
- the material there may be mentioned, for example, polyethylene, polypropylene, polymethylpentene, polycarbonate, polyurethane, Teflon (trade name, produced by E.I. du Pont de Nemours & Co.
- rubbers e.g., butadiene rubber, styrene-butadiene rubber and silicone rubber
- polyvinyl chloride polyvinyl acetate, polyvinylidene chloride, polystyrene, polyvinyltoluene, polyacrylate, polymethacrylate, a copolymer of ethylene and vinyl acetate, a copolymer of ethylene and acrylate, a copolymer of vinyl chloride and vinyl acetate, a copolymer of styrene and acrylate or methacrylate, a copolymer of vinyltoluene and acrylate or methacrylate, a polyvinyl alcohol type resin (e.g., a hydrolyzate of polyacrylate or polymethacrylate, a hydrolyzate of polyvinyl acetate, a hydrolyzate of a copolymer of ethylene and vinyl acetate, a hydrolyzate of a copolymer
- the embedding layer (C) in the present invention may be also constituted by a resin composition comprising the material constituting the embedding layer (C) and a photopolymerization initiator which produces free radical by irradiation of active light.
- the photopolymerization initiator which produces free radical by irradiation of active light there may be used the above photopolymerization initiator (c) which produces free radical by irradiation of active light, which can be used in the photosensitive resin composition constituting the phosphor-containing photosensitive resin composition layer (A).
- the embedding layer (C) in the present invention may be also constituted by a resin composition comprising the material constituting the embedding layer (C) and a photopolymerizable unsaturated compound having an ethylenic unsaturated group.
- the photopolymerizable unsaturated compound having an ethylenic unsaturated group there may be used the above photopolymerizable unsaturated compound (b) having an ethylenic unsaturated group, which can be used in the photosensitive resin composition constituting the phosphor-containing photosensitive resin composition layer (A).
- polyethylene, polypropylene, Teflon or the like formed into a film shape by a melt extrusion method or the like may be used as the embedding layer (C).
- the embedding layer (C) in the present invention can be also obtained as a film or a sheet by dissolving the above resin and others constituting the embedding layer (C) in or mixing the above resin and others with a solvent which can dissolve or disperse the above resin and others to prepare a solution in which the above resin and others are dissolved or dispersed uniformly and coating the solution of the support film described above, followed by drying.
- a coating method a known method may be used, and there may be mentioned, for example, a knife coating method, a roll coating method, a spray coating method, a gravure coating method, a bar coating method and a curtain coating ) method.
- the drying temperature is preferably 60 to 130 °C, and the drying time is preferably 3 minutes to 1 hour.
- the thickness of the embedding (C) in the present invention is not particularly limited, but it is preferably 10 to 200 ⁇ m, more preferably 15 to 150 ⁇ m, particularly preferably 20 to 100 ⁇ m. If the thickness is less than 10 ⁇ m, a phosphor pattern after calcination described below tends to be thin to lower light emission efficiency, while if it exceeds 200 ⁇ m, a phosphor pattern after calcination tends to be thick to reduce a light emission area of a phosphor surface, which results in lowering of light emission efficiency.
- the viscosity at 100 °C of the embedding layer (C) in the present invention is preferably 1 to 1 x 10 9 Pa ⁇ sec, more preferably 2 to 1 x 10 8 Pa ⁇ sec, particularly preferably 5 to 1 x 10 7 Pa ⁇ sec, extremely preferably 10 to 1 x 10 6 Pa ⁇ sec. If the viscosity at 100 °C is less than 1 Pa ⁇ sec, the viscosity at room temperature becomes too low so that when a photosensitive element is prepared, the embedding layer (C) tends to be exuded from an edge portion by flowing, and film-forming property tends to be lowered.
- the above peelable cover film may be further laminated. It is preferred that the adhesive strength of the cover film to the embedding layer (C) is smaller than the adhesive strength of the support film to the embedding layer (C).
- a film or the like for facilitating separation of the embedding layer (C) from the phosphor-containing photosensitive resin composition layer (A), in which the adhesive strength to the phosphor-containing photosensitive resin composition layer (A) to the cover film is smaller than the adhesive strength to the embedding layer (C) may be laminated between the embedding layer (C) and the cover film.
- the embedding layer (C) having a film shape or sheet shape as described above can be stored by being wound in a roll state.
- the respective steps of the process for preparing a phosphor pattern of the present invention including (Ic) a step of heating and pressurizing an embedding layer (C) in a state that the embedding layer (C) is superposed on the phosphor-containing photosensitive resin composition layer (A) on an uneven surface of a substrate having unevenness, to laminate the phosphor-containing photosensitive resin composition layer (A) and the embedding layer (C) on the uneven surface; (IIc) a step of peeling the embedding layer (C); (IIIc) a step of irradiating the phosphor-containing photosensitive resin composition layer (A) imagewisely with active light; (IVc) a step of removing an unnecessary portion from the phosphor-containing photosensitive resin composition layer (A) by development; and (Vc) a step of removing unnecessary components from the phosphor-containing photosensitive resin composition layer (A) by calcination are explained in detail by referring to Fig. 15 and Fig. 16. Fig. 15 and
- Fig. 15 (a) and Fig. 15 (b) each show one embodiment of the step (Ic) of heating and pressurizing an embedding layer (C) in a state that the embedding layer (C) is superposed on the phosphor-containing photosensitive resin composition layer (A) on an uneven surface of a substrate having unevenness, to laminate the phosphor-containing photosensitive resin composition layer (A) and the embedding layer (C) on the uneven surface.
- Fig. 15 (a) shows a state that the phosphor-containing photosensitive resin composition layer (A) 7 is laminated on the substrate 1 for PDP (the substrate having unevenness) on which the barrier rib 2 is formed.
- a method for laminating the phosphor-containing photosensitive resin composition layer (A) 7 on the substrate 1 for PDP on which the barrier rib 2 is formed there may be mentioned, for example, the above lamination method by using the photosensitive element.
- the photosensitive element when a cover film exists on the photosensitive element, after the cover film is removed, the photosensitive element can be laminated by contact bonding using a contact bonding roll or the like so that the phosphor-containing photosensitive resin composition layer (A) 7 is contacted with the surface on which the barrier rib is formed, of the substrate for PDP.
- the contact bonding pressure when pressurization is carried out is preferably 50 to 1 x 10 5 N/m, more preferably 2.5 x 10 2 to 5 x 10 4 N/m, particularly preferably 5 x 10 2 to 4 x 10 4 N/m in terms of line pressure. If the contact bonding pressure is less than 50 N/m, property of embedding the phosphor-containing photosensitive resin composition layer (A) 7 in the space of a concave portion of the substrate for PDP tends to be lowered, while if it exceeds 1 x 10 5 N/m, the barrier rib on the substrate for PDP tends to be broken.
- the above contact bonding roll having a surface made of a material abundant in flexibility, such as rubber and plastics may be used.
- the thickness of the layer of the material abundant in flexibility is preferably 200 to 400 ⁇ m.
- lamination may be carried out by contact bonding of the photosensitive element to the surface on which the barrier rib is formed, of the substrate for PDP while heating the photosensitive element by a heating roll or the like.
- the heating temperature at the time of contact bonding under heating is preferably 10 to 140 °C, more preferably 20 to 135 °C, particularly preferably 30 to 130 °C. If the heating temperature is lower than 10 °C, the phosphor-containing photosensitive resin composition layer (A) 7 tends not to be adhered to the substrate for PDP sufficiently, while if it exceeds 140 °C, the phosphor-containing photosensitive resin composition layer (A) 7 tends to be thermoset.
- the contact bonding pressure at the time of contact bonding under heating is preferably 50 to 1 x 10 5 N/m, more preferably 2.5 x 10 2 to 5 x 10 4 N/m, particularly preferably 5 x 10 2 to 4 x 10 4 N/m in terms of line pressure. If the contact bonding pressure is less than 50 N/m, property of embedding the phosphor-containing photosensitive resin composition layer (A) 7 in the space of the concave portion of the substrate for PDP tends to be lowered, while if it exceeds 1 x 10 5 N/m, the barrier rib on the substrate for PDP tends to be broken.
- the preheating temperature is preferably 30 to 130 °C, and the preheating time is preferably 0.5 to 20 minutes.
- operations of the above contact bonding and contact bonding under heating may be carried out under a reduced pressure of 5 x 10 4 Pa or less.
- heating may be carried out at a temperature range of 30 to 150 °C for 1 to 120 minutes. At the time of heating, a support film may be removed, if necessary.
- the phosphor-containing photosensitive resin composition layer (A) 7 can be laminated on the substrate 1 for PDP on which the barrier rib 2 is formed.
- Fig. 15 (b) shows a state that an embedding layer (C) 14 is superposed on the phosphor-containing photosensitive resin composition layer (A) 7, and contact bonding of the embedding layer (C) 14 is carried out to embed the phosphor-containing photosensitive resin composition layer (A) 7 and the embedding layer (C) 14 in a space surrounded with the wall surface of the barrier rib 2 of the substrate 1 (the substrate having unevenness) for PDP on which said barrier rib is formed and the bottom of said substrate.
- a method for superposing the embedding layer (C) 14 on the phosphor-containing photosensitive resin composition layer (A) 7 and carrying out contact bonding there may be mentioned, for example, a method in which when a support film exists on the phosphor-containing photosensitive resin composition layer (A) 7 in the state of Fig. 15 (a), after the support film is removed, (when a cover film exists on the embedding layer (C) 14, after the cover film is removed), the embedding layer (C) 14 is superposed on the phosphor-containing photosensitive resin composition layer (A) 7, and contact bonding is carried out by a contact bonding roll or the like.
- contact bonding may be carried out by the contact bonding roll or the like while removing the support film, if necessary.
- the contact bonding pressure at the time of contact bonding under heating is preferably 50 to 1 x 10 5 N/m, more preferably 2.5 x 10 2 to 5 x 10 4 N/m, particularly preferably 5 x 10 2 to 4 x 10 4 N/m in terms of line pressure. If the contact bonding pressure is less than 50 N/m, property of embedding the phosphor-containing photosensitive resin composition layer (A) 7 in the space of the concave portion of the substrate for PDP tends to be lowered, while if it exceeds 1 x 10 5 N/m, the barrier rib on the substrate for PDP tends to be broken.
- the above contact bonding roll having a surface made of a material abundant in flexibility, such as rubber and plastics may be used.
- the thickness of the layer of the material abundant in flexibility is preferably 200 to 400 ⁇ m.
- lamination may be carried out by contact bonding of the embedding layer (C) 14 to the surface on which the barrier rib is formed, of the substrate for PDP while heating the embedding layer (C) 14 by a heating roll 9 or the like.
- the heating temperature when heating is carried out is preferably 10 to 140 °C, more preferably 20 to 135 °C, particularly preferably 30 to 130 °C. If the heating temperature is lower than 10 °C, property of embedding the phosphor-containing photosensitive resin composition layer (A) 7 in the space of the substrate for PDP tends to be lowered, while if it exceeds 140 °C, the phosphor-containing photosensitive resin composition layer (A) 7 tends to be thermoset.
- the embedding layer (C) 14 When the embedding layer (C) 14 is heated as described above, it is not necessary to carry out preheat treatment of the substrate for PDP on which the phosphor-containing photosensitive resin composition layer (A) 7 is laminated. However, from the point that property of embedding the phosphor-containing photosensitive resin composition layer (A) 7 in the space of the concave portion is further improved, it is preferred to carry out preheat treatment of the substrate for PDP on which the phosphor-containing photosensitive resin composition layer (A) 7 is laminated.
- the preheating temperature is preferably 30 to 130 °C, and the preheating time is preferably 0.5 to 20 minutes.
- the above contact bonding roll under heating having a surface made of a material abundant in flexibility, such as rubber and plastics may be used.
- the thickness of the layer of the material abundant in flexibility is preferably 200 to 400 ⁇ m.
- operations of the above contact bonding and contact bonding under heating may be carried out under a reduced pressure of 5 x 10 4 Pa or less.
- heating may be carried out at a temperature range of 30 to 150 °C for 1 to 120 minutes.
- the support film may be removed, if necessary.
- the phosphor-containing photosensitive resin composition layer (A) 7 can be formed uniformly in the space of the substrate for PDP.
- both of the phosphor-containing photosensitive resin composition layer (A) 7 and the embedding layer (C) 14 may be laminated simultaneously which carrying out contact bonding under heating.
- the substrate for PDP may be cooled (generally in a range of -50 to 50 °C) after the step of (Ic).
- the layers can be laminated in a state as shown in Fig. 16.
- the layer thicknesses of the phosphor-containing photosensitive resin composition layer (A) 7 and the embedding layer (C) 14 from the point that a phosphor pattern with high precision and a uniform shape can be formed, it is preferred that in the phosphor-containing photosensitive resin composition layer (A) and the embedding layer (C) in a region which is the same as the region where unevenness is formed on a substrate having unevenness, the ratio (V' 1 )/(V' 2 ) of the total volume (V' 1 ) of the phosphor-containing photosensitive resin composition layer (A) and the embedding layer (C) to the volume (V' 2 ) of the space of a concave portion of the substrate having unevenness is in the range of 1 to 2.
- the phosphor-containing photosensitive resin composition layer (A) 7 tends to be formed on the inner surface of the concave portion in a state that almost none of the phosphor-containing photosensitive resin composition layer (A) 7 remains on the convex portion as shown in Fig. 15 (b). If (V' 1 )/(V' 2 ) exceeds 1.05 and is 2 or less, the phosphor-containing photosensitive resin composition layer (A) 7 tends to be formed on the inner surface of the concave portion in a state that the phosphor-containing photosensitive resin composition layer (A) 7 remains on the convex portion as shown in Fig. 16.
- the phosphor-containing photosensitive resin composition layer (A) 7 is laminated on the inner surface of the concave portion so that almost none of the phosphor-containing photosensitive resin composition layer (A) 7 remains on the convex portion as shown in Fig. 15 (b).
- lamination may be carried out as shown in Fig. 15 (b), or lamination may be carried out in a state that the phosphor-containing photosensitive resin composition layer (A) 7 remains on the convex portion as shown in Fig. 16.
- the phosphor-containing photosensitive resin composition layer (A) 7 can be formed on the inner surface (the wall surface of the barrier rib 2 and the surface of the substrate 1 ) of the substrate having unevenness (the substrate for PDP) with a good shape and good operatability.
- Fig. 15 (c) shows a state that the embedding layer (C) 14 is peeled off.
- a method for peeling the embedding layer (C) 14 there may be mentioned, for example, a method of peeling the embedding layer (C) 14 physically by adhering an adhesive tape on the embedding layer (C) 14 or using a hook-shaped jig or the like.
- the embedding layer (C) 14 may be wound by using a winding roll or the like.
- the phosphor-containing photosensitive resin composition layer (A) 7 can be formed on the inner surface (the wall surface of the barrier rib 2 and the surface of the substrate 1) of the concave portion of the substrate having unevenness (the substrate for PDP) with a good shape and good operatability.
- Fig. 15 (d) shows a state that active light 11 is irradiated imagewisely.
- a method for irradiating the active light 11 imagewisely there may be used a method of irradiating the active light 11 imagewisely through a photomask 10 such as a negative film and a positive film, provided above the phosphor-containing photosensitive resin-composition layer (A) 7 in the state of Fig. 15 (c).
- a photomask 10 such as a negative film and a positive film
- the active light 11 may be also irradiated imagewisely after the phosphor-containing photosensitive resin composition layer (A) 7 is newly covered with the support film described above.
- the above step (IIc) of peeling the embedding layer (C) may be carried out after this step (IIIc) is carried out in a state that the embedding layer (C) 14 is superposed.
- the permeation width of the active light 11 of the photomask 10 is the same permeation width as the opening width of the concave portion of the substrate for PDP or wider than the opening width of the concave portion of the substrate for PDP.
- photomask 10 has an active light permeation width which is narrower than the opening width of the concave portion.
- the active light permeation width which is narrower than the opening width of the concave portion is preferably 0.3 x W to 0.99999 x W, more preferably 0.5 x W to 0.999 x W, particularly preferably 0.6 x W to 0.99 x W.
- the active light permeation width which is narrower than the opening width of the concave portion is less than 0.3 x W, photocuring of the phosphor-containing photosensitive resin composition layer (A) 7 formed on the inner surface of the concave portion tends to be insufficient.
- developing solution resistance (property that a portion which remains without being removed by development and becomes a pattern is not corroded by development) of the phosphor-containing photosensitive resin composition layer (A) 7 formed on the inner surface of the concave portion tends to be lowered, and even a necessary portion of the phosphor-containing photosensitive resin composition layer (A) 7 formed on the inner surface of the concave portion tends to be removed.
- the active light permeation width which is narrower than the opening width of the concave portion is a width exceeding 0.99999 x W, even a portion other than the inner surface of the concave portion to be photocured tends to be photocured, and an unnecessary portion tends to remain after development described below.
- the active light 11 a known active light source may be used, and there may be mentioned, for example, light generated from carbon arc, mercury vapor arc, xenon arc or the like.
- the sensitivity of a photopolymerization initiator is generally the largest in a UV ray region so that in that case, an active light source which radiates UV ray-effectively should be used.
- an active light source which radiates UV ray-effectively should be used.
- the photopolymerization initiator is sensitive to visible rays, for example, it is 9,10-phenanthrenequinone, visible light can be used as the active light 11, and as a light source thereof, there may be also used, in addition to the above light sources, a flood bulb for photographs and a solar lamp.
- parallel light non-parallel light and scattered light.
- parallel light non-parallel light or scattered light
- one or two or all of them may be used in one step, and two of them may be used in two stages or all of them may be used in all stages separately.
- two of them are used in two stages or all of them are used in all stages separately, either of them may be used firstly.
- the irradiation dose of the active light 11 is preferably 3 mJ/cm 2 to 3 J/cm 2 , more preferably 5 mJ/cm 2 to 1 J/cm 2 , particularly preferably 10 mJ/cm 2 to 1 J/cm 2 .
- active light can be irradiated imagewisely with high precision and good operatability.
- thermoplastic resin layer (B) As a method for removing an unnecessary portion from the phosphor-containing photosensitive resin composition layer (A) by development, there may be used all of the same methods as in the above step (IIIa) of removing unnecessary portions from the phosphor-containing photosensitive resin composition layer (A) and/or the thermoplastic resin layer (B) by development.
- step (IVa) of removing unnecessary components from the phosphor-containing photosensitive resin composition layer (A) and/or the thermoplastic resin layer (B) by calcination there may be used all of the same methods as in the above step (IVa) of removing unnecessary components from the phosphor-containing photosensitive resin composition layer (A) and/or the thermoplastic resin layer (B) by calcination.
- a multicolor pattern comprising photosensitive resin composition layers each containing a phosphor which emits red, green or blue light is formed by repeating the respective steps of (Ic) to (IVc) of the above process of the present invention for every color, the step of (Vc) is carried out to form a multicolor phosphor pattern.
- pattern formations of red, blue and green may be carried out in any order.
- a multicolor phosphor pattern which emit red, green and blue lights is formed by repeating the respective steps of (Ic) to (Vc) in the above process of the present invention for every color.
- the photosensitive element in the present invention has a support film, the embedding layer (C) on the support film and the phosphor-containing photosensitive resin composition layer (A) thereon.
- the photosensitive element in the present invention can be obtained by dissolving the above resin constituting the embedding layer (C) in or mixing said resin with a solvent which dissolves said resin to prepare a uniform solution, coating the solution on the above support film by using a known coating method such as a knife coating method, a roll coating method, a spray coating method, a gravure coating method, a bar coating method and a curtain coating method, followed by drying, dissolving the above respective components constituting the phosphor-containing photosensitive resin composition layer (A) in or mixing said components with a solvent which can dissolve or disperse said components to prepare a solution in which said components are dispersed uniformly and coating the solution on the embedding layer (C) provided as described above by using a known coating method such as a knife coating method, a roll coating method, a spray coating method, a gravure coating method, a bar coating method and a curtain coating method, followed by drying.
- a known coating method such as a knife coating method, a roll coating method, a spray
- the solvent which dissolves the resin constituting the embedding layer (C) and the above respective components constituting the phosphor-containing photosensitive resin composition layer (A) there may be mentioned, for example, water, toluene, acetone, methyl ethyl ketone,'methyl isobutyl ketone, methyl cellosolve, ethyl cellosolve, ⁇ -butyrolactone, N-methylpyrrolidone, dimethylformamide, tetramethylsulfone, diethylene glycol dimethyl ether, diethylene glycol monobutyl ether, chloroform, methylene chloride, methyl alcohol and ethyl alcohol. These solvents are used singly or in combination of two or more of them.
- the material of a portion of a coating apparatus, contacted with the solution in which the above respective components constituting the phosphor-containing photosensitive resin composition layer (A) are dispersed uniformly by dissolving said components in or mixing said components with the solvent which can dissolve or disperse said components is preferably a non-metallic material.
- the coating apparatus contacted with the solution constituting the phosphor-containing photosensitive resin composition layer (A) is polished by the phosphor in said solution, and powder generated by polishing tends to migrate, as impurity, into the solution constituting the phosphor-containing photosensitive resin composition layer (A) .
- the drying temperature is preferably 60 to 130 °C, and the drying time is preferably 3 minutes to 1 hour.
- the thickness of the phosphor-containing photosensitive resin composition layer (A) in the present invention is not particularly limited, but it is preferably 10 to 200 ⁇ m, more preferably 15 to 150 ⁇ m, particularly preferably 20 to 100 ⁇ m. If the thickness is less than 10 ⁇ m, a phosphor pattern after calcination described below tends to be thin to lower light emission efficiency, while if it exceeds 200 ⁇ m, a phosphor pattern after calcination tends to be thick to reduce a light emission area of a phosphor surface, which results in lowering of light emission efficiency.
- the thickness of the embedding layer (C) in the present invention is not particularly limited, but it is preferably 10 to 200 ⁇ m, more preferably 15 to 150 ⁇ m, particularly preferably 20 to 100 ⁇ m. If the thickness is less than 10 ⁇ m, a phosphor pattern after calcination described below tends to be thin to lower light emission efficiency, while if it exceeds 200 ⁇ m, a phosphor pattern after calcination tends to be thick to reduce a light emission area of a phosphor surface, which results in lowering of light emission efficiency.
- the above peelable cover film may be further laminated.
- the cover film there may be mentioned polyethylene, polypropylene, polyethylene terephthalate and polycarbonate. It is preferred that the adhesive strength of the cover film to the phosphor-containing photosensitive resin composition layer (A) is smaller than the adhesive strength of the support film to the embedding layer (C) and the adhesive strength of the embedding layer (C) to the phosphor-containing photosensitive resin composition layer (A).
- the photosensitive element of the present invention can be also obtained by coating the solution in which the above respective components constituting the phosphor-containing photosensitive resin composition layer (A) are dispersed uniformly obtained by dissolving said components in or mixing said components with the above solvent which can dissolve or disperse said components, on the above support film by using a known coating method such as a knife coating method, a roll coating method, a spray coating method, a gravure coating method, a bar coating method and a curtain coating method, followed by drying, to form the phosphor-containing photosensitive resin composition layer (A) and then pasting the phosphor-containing photosensitive resin composition layer (A) and the embedding layer (C) provided on the above support film so that both layers are contacted.
- a known coating method such as a knife coating method, a roll coating method, a spray coating method, a gravure coating method, a bar coating method and a curtain coating method, followed by drying, to form the phosphor-containing photosensitive resin composition layer (A) and then pasting the
- the adhesive strength of the support film with which the phosphor-containing photosensitive resin composition layer (A) is contacted to the phosphor-containing photosensitive resin composition layer (A) is smaller than the adhesive strength of the support film with which the embedding layer (C) is contacted to the embedding layer (C) and the adhesive strength of the embedding layer (C) to the phosphor-containing photosensitive resin composition layer (A).
- the photosensitive element of the present invention obtained as described above can be stored by being wound in a roll state.
- the respective steps of the process for preparing a phosphor pattern of the present invention including (Id) a step of heating and pressurizing a photosensitive element having a support film, the embedding layer (C) provided on the support film and the phosphor-containing photosensitive resin composition layer (A) provided thereon so that the phosphor-containing photosensitive resin composition layer (A) is contacted with an uneven surface of a substrate having unevenness, to laminate the phosphor-containing photosensitive resin composition layer (A) and the embedding layer (C) on the uneven surface; (IId) a step of peeling the embedding layer (C); (IIId) a step of irradiating the phosphor-containing photosensitive resin composition layer (A) imagewisely with active light; (IVd) a step of removing an unnecessary portion from the phosphor-containing photosensitive resin composition layer (A) by development; and (Vd) a step of removing unnecessary components from the phosphor-containing photosensitive resin composition layer (A) by
- Fig. 16 shows a state that the photosensitive element of the present invention including the embedding layer (C) 14 and the phosphor-containing photosensitive resin composition layer (A) 7 is laminated by using a heating roll 9, on the uneven surface of the above substrate 1 for PDP (the substrate having unevenness) on which the barrier rib 2 is formed.
- a method for laminating the photosensitive element of the present invention including the embedding layer (C) 14 and the phosphor-containing photosensitive resin composition layer (A) 7 on the substrate 1 for PDP on which the barrier rib 2 is formed there may be mentioned, for example, a method in which when a cover film exists on the photosensitive element, after the cover film is removed (when a photosensitive element obtained by pasting the embedding layer (C) 14 formed on a support film and the phosphor-containing photosensitive resin composition layer (A) 7 formed on a support film is used, after the support film of the phosphor-containing photosensitive resin composition layer (A) 7 is removed), lamination is carried out by contact bonding under heating of the photosensitive element by the heating roll 9 so that the phosphor-containing photosensitive resin composition layer (A) 7 is contacted with the surface on which the barrier rib 2 is formed, of the substrate 1 for PDP.
- the heating temperature at the time of contact bonding under heating is preferably 10 to 140 °C, more preferably 20 to 135 °C, particularly preferably 30 to 130 °C. If the heating temperature is lower than 10 °C, property of embedding the phosphor-containing photosensitive resin composition layer (A) 7 in the space of the substrate for PDP tends to be lowered, while if it exceeds 140 °C, the phosphor-containing photosensitive resin composition layer (A) 7 tends to be thermoset.
- the contact bonding pressure at the time of contact bonding under heating is preferably 50 to 1 x 10 5 N/m, more preferably 2.5 x 10 2 to 5 x 10 4 N/m, particularly preferably 5 x 10 2 to 4 x 10 4 N/m in terms of line pressure. If the contact bonding pressure is less than 50 N/m, property of embedding the phosphor-containing photosensitive resin composition layer (A) 7 in the space of the concave portion of the substrate for PDP tends to be lowered, while if it exceeds 1 x 10 5 N/m, the barrier rib on the substrate for PDP tends to be broken.
- the photosensitive element of the present invention including the embedding layer (C) 14 and the phosphor-containing photosensitive resin composition layer (A) 7 is heated as described above, it is not necessary to carry out preheat treatment of the substrate for PDP. However, from the point that property of embedding the phosphor-containing photosensitive resin composition layer (A) 7 in the space of the concave portion is further improved, it is preferred to carry out preheat treatment of the substrate for PDP.
- the preheating temperature is preferably 30 to 140 °C, and the preheating time is preferably 0.5 to 20 minutes.
- the above heating roll 9 having a surface made of a material abundant in flexibility, such as rubber and plastics may be used.
- the thickness of the layer of the material abundant in flexibility is preferably 200 to 400 ⁇ m.
- operations of the above contact bonding and contact bonding under heating may be carried out under a reduced pressure of 5 x 10 4 Pa or less.
- heating may be carried out at a temperature range of 30 to 150 °C for 1 to 120 minutes.
- the support film may be removed, if necessary.
- the phosphor-containing photosensitive resin composition layer (A) 7 can be formed uniformly in the space of the concave portion of the substrate for PDP.
- the substrate for PDP may be cooled (generally in a range of -50 to 50 °C) after the step of (Id) .
- the layers can be laminated in a state as shown in Fig. 16.
- the layer thicknesses of the phosphor-containing photosensitive resin composition layer (A) 7 and the embedding layer (C) 14 from the point that a phosphor pattern with high precision and a uniform shape can be formed, it is preferred that in the phosphor-containing photosensitive resin composition layer (A) and the embedding layer (C) in a region which is the same as the region where unevenness is formed on a substrate having unevenness, the ratio (V' 1 )/(V' 2 ) of the total volume (V' 1 ) of the phosphor-containing photosensitive resin composition layer (A) and the embedding layer (C) to the volume (V' 2 ) of the space of a concave portion of the substrate having unevenness is in the range of 1 to 2.
- the phosphor-containing photosensitive resin composition layer (A) 7 tends to be formed on the inner surface of the concave portion in a state that almost none of the phosphor-containing photosensitive resin composition layer (A) 7 remains on the convex portion as shown in Fig. 17. If (V' 1 )/(V' 2 ) exceeds 1.05 and is 2 or less, the phosphor-containing photosensitive resin composition layer (A) 7 tends to be formed on the inner surface of the concave portion in a state that the phosphor-containing photosensitive resin composition layer (A) 7 remains on the convex portion as shown in Fig. 16.
- the phosphor-containing photosensitive resin composition layer (A) 7 is laminated on the inner surface of the concave portion so that almost none of the phosphor-containing photosensitive resin composition layer (A) 7 remains on the convex portion as shown in Fig. 17.
- lamination may be carried out as shown in Fig. 17, or lamination may be carried out in a state that the phosphor-containing photosensitive resin composition layer (A) 7 remains on the convex portion as shown in Fig. 16.
- the phosphor-containing photosensitive resin composition layer (A) 7 can be laminated uniformly on the surface (on the uneven surface) of the substrate 1 for PDP on which the barrier rib 2 is formed.
- a multicolor pattern comprising photosensitive resin composition layers each containing a phosphor which emits red, green or blue light is formed by repeating the respective steps of (Id) to (IVd) of the above process of the present invention for every color, the step of (Vd) is carried out to form a multicolor phosphor pattern.
- pattern formations of red, blue and green may be carried out in any order.
- a multicolor phosphor pattern which emit red, green and blue lights is formed by repeating the respective steps of (Id) to (Vd) in the above process of the present invention for every color.
- Fig. 18 is a schematical view showing the respective steps of the process for preparing a phosphor pattern of the present invention.
- Step.of pressurizing the phosphor-containing photosensitive resin composition layer (A) in a state that the phosphor-containing photosensitive resin composition layer (A) is superposed on a substrate having unevenness, to adhere the phosphor-containing photosensitive resin composition layer (A) to the inner surface of a concave portion on the substrate having unevenness>
- a method for adhering the phosphor-containing photosensitive resin composition layer (A) 7 to a substrate having unevenness in a state that the phosphor-containing photosensitive resin composition layer (A) 7 is superposed on the substrate while applying pressure in the present invention there may be mentioned, for example, a method of applying atmospheric pressure, wind pressure, hydraulic pressure or the like, a method of carrying out pressurization using a roll having a surface made of a soft and elastic material such as a sponge, rubber, polyethylene, polymethylpentene and a blend of polyethylene and an acryl resin, a method of carrying out pressurization entirely and uniformly by placing a sheet made of a soft and elastic material such as a sponge, rubber, polyethylene, polymethylpentene and a blend of polyethylene and an acryl resin thereon, a method of reducing pressure in a space surrounded with the substrate 1 for PDP, the barrier rib 2 and the phosphor-containing photosensitive resin composition layer (A) 7 to embed the phosphor-containing photosensitive resin composition layer
- a support film existing on the phosphor-containing photosensitive resin composition layer (A) 7 is generally removed, but adhering may be carried out in a state that the support film exists thereon.
- the photopolymerizable unsaturated compound (b) having an ethylenic unsaturated group constituting the phosphor-containing photosensitive resin composition layer (A) 7 is a photopolymerizable unsaturated compound
- its boiling point (760 mmHg) is preferably 300 °C or higher, more preferably 350 °C or higher, particularly preferably 400 °C or higher, from the points of stability and operatability when heating is carried out under reduced pressure.
- the weight average molecular weight of the photopolymerizable unsaturated compound (b) having an ethylenic unsaturated group constituting the phosphor-containing photosensitive resin composition layer (A) 7 is not particularly limited, but it is preferably 400 or more, more preferably 500 or more, particularly preferably 600 or more, from the points of stability and operatability when heating is carried out under reduced pressure.
- application of pressure may be accompanied with heating.
- Fig. 18 and Fig. 19 each show an example of a state that the phosphor-containing photosensitive resin composition layer (A) 7 in the present invention is adhered to the inner surface of the concave portion on the substrate having unevenness by applying pressure.
- a method for adhering the phosphor-containing photosensitive resin composition layer (A) 7 to the inner surface of the concave portion there may be mentioned, for example, a method in which when a cover film exists on a photosensitive element including the phosphor-containing photosensitive resin composition layer (A) 7, after the cover film is removed, and the phosphor-containing photosensitive resin composition layer (A) 7 is adhered to the inner surface of the concave portion of the above substrate for PDP so that the phosphor-containing photosensitive resin composition layer (A) 7 is contacted with the surface on which the barrier rib 2 is formed, of the substrate for PDP while applying pressure by a roll or the like on the phosphor-containing photosensitive resin composition layer (A) 7.
- the pressure when adhesion is carried out by pressurization using the above roll or the like is preferably 50 to 1 x 10 5 N/m, more preferably 2.5 x 10 2 to 5 x 10 4 N/m, particularly preferably 5 x 10 2 to 4 x 10 4 N/m in terms of line pressure. If the adhesion pressure is less than 50 N/m, property of embedding the phosphor-containing photosensitive resin composition layer (A) 7 in the space of the concave portion of the substrate for PDP tends to be lowered, while if it exceeds 1 x 10 5 N/m, the barrier rib on the substrate for PDP tends to be broken.
- the temperature when application of pressure is accompanied with heating is preferably 10 to 140 °C, more preferably 20 to 135 °C, particularly preferably 30 to 130 °C. If the temperature is lower than 10 °C, property of embedding the phosphor-containing photosensitive resin composition layer (A) 7 in the space of the concave portion of the substrate for PDP tends to be lowered, while if it exceeds 140 °C, the phosphor-containing photosensitive resin composition layer (A) 7 tends to be cured.
- the phosphor-containing photosensitive resin composition layer (A) 7 When the phosphor-containing photosensitive resin composition layer (A) 7 is heated as described above, it is not necessary to carry out preheat treatment of the substrate 1 for PDP. However, from the point that embedding property for adhering the phosphor-containing photosensitive resin composition layer (A) 7 to the inner surface of the concave portion is further improved, it is preferred to carry out preheat treatment of the above substrate 1 for PDP.
- the preheating temperature is preferably 30 to 130 °C, and the preheating time is preferably 0.5 to 20 minutes.
- heating may be carried out at a temperature range of 30 to 150 °C for 1 to 120 minutes. At the time of heating, when a support film exists on the phosphor-containing photosensitive resin composition layer (A) 7, the support film may be removed, if necessary.
- the phosphor-containing photosensitive resin composition layer (A) 7 may be laminated so that it is contacted with the surface on which the barrier rib 2 is formed, of the substrate 1 for PDP, or the phosphor-containing photosensitive resin composition layer (A) 7 may be laminated and adhered to the inner surface of the concave portion while applying pressure in one step.
- lamination may be carried out only by superposing the phosphor-containing photosensitive resin composition layer (A) 7 on the surface on which the barrier rib 2 is formed, of the substrate 1 for PDP, may be carried out under pressurization or may be carried out under a reduced pressure of 5 x 10 4 or less. Also, lamination may be accompanied with heating.
- the pressure when pressurization is carried out is preferably 50 to 1 x 10 5 N/m, more preferably 2.5 x 10 2 to 5 x 10 4 N/m, particularly preferably 5 x 10 2 to 4 x 10 4 N/m in terms of line pressure.
- the temperature when application of pressure is accompanied with heating is preferably 10 to 140 °C, more preferably 20 to 135 °C, particularly preferably 30 to 130 °C.
- a method for adhering the phosphor-containing photosensitive resin composition layer (A) 7 to the inner surface of the concave portion there may be mentioned, for example, a method in which after the phosphor-containing photosensitive resin composition layer (A) 7 is laminated on the substrate 1 for PDP and pressure is reduced to 5 to 500 Pa, pressure is made atmospheric pressure in a state that a space surrounded with the substrate 1 for PDP, the barrier rib 2 and the phosphor-containing photosensitive resin composition layer (A) 7 is closed tightly, to embed the phosphor-containing photosensitive resin composition layer (A) 7 in the space of the concave portion of the substrate for PDP by atmospheric pressure.
- a method for laminating the phosphor-containing photosensitive resin composition layer (A) 7 on the substrate 1 for PDP on which the barrier rib 2 is formed there may be mentioned, for example, the above lamination method by using the photosensitive element constituted by the phosphor-containing photosensitive resin composition layer (A) .
- the photosensitive element when a cover film exists on the photosensitive element, after the cover film is removed, the photosensitive element can be laminated by contact bonding using a contact bonding roll or the like so that the phosphor-containing photosensitive resin composition layer (A) 7 is contacted with the surface on which the barrier rib is formed, of the substrate for PDP.
- the contact bonding pressure when pressurization is carried out is preferably 50 to 1 x 10 5 N/m, more preferably 2.5 x 10 2 to 5 x 10 4 N/m, particularly preferably 5 x 10 2 to 4 x 10 4 N/m in terms of line pressure. If the contact bonding pressure is less than 50 N/m, property of embedding the phosphor-containing photosensitive resin composition layer (A) 7 in the space of the concave portion of the substrate for PDP tends to be lowered, while if it exceeds 1 x 10 5 N/m, the barrier rib on the substrate for PDP tends to be broken.
- the above contact bonding roll having a surface made of a material abundant in flexibility, such as rubber and plastics may be used.
- the thickness of the layer of the material abundant in flexibility is preferably 200 to 400 ⁇ m.
- lamination may be carried out by contact bonding of the photosensitive element to the surface on which the barrier rib is formed, of the substrate for PDP while heating the photosensitive element by a heating roll or the like.
- the heating temperature at the time of contact bonding under heating is preferably 10 to 140 °C, more preferably 20 to 135 °C, particularly preferably 30 to 130 °C. If the heating temperature is lower than 10 °C, the phosphor-containing photosensitive resin composition layer (A) 7 tends not to be adhered to the substrate for PDP sufficiently, while if it exceeds 140 °C, the phosphor-containing photosensitive resin composition layer (A) 7 tends to be thermoset.
- the contact bonding pressure at the time of contact bonding under heating is preferably 50 to 1 x 10 5 N/m, more preferably 2.5 x 10 2 to 5 x 10 4 N/m, particularly preferably 5 x 10 2 to 4 x 10 4 N/m in terms of line pressure. If the contact bonding pressure is less than 50 N/m, property of embedding the phosphor-containing photosensitive resin composition layer (A) 7 in the space of the concave portion of the substrate for PDP tends to be lowered, while if it exceeds 1 x 10 5 N/m, the barrier rib on the substrate for PDP tends to be broken.
- the preheating temperature is preferably 30 to 130 °C, and the preheating time is preferably 0.5 to 20 minutes.
- operations of the above contact bonding and contact bonding under heating may be carried out under a reduced pressure of 5 x 10 4 Pa or less.
- the phosphor-containing photosensitive resin composition layer (A) 7 is superposed on the surface on which the barrier rib 2 is formed, of the substrate 1 for PDP so that air passage through which air in a space 16 (a discharge space) surrounded with the substrate 1 for PDP, the barrier rib 2 and the phosphor-containing photosensitive resin composition layer (A) 7 can be exhausted in the step of reducing pressure described below is left.
- the phosphor-containing photosensitive resin composition layer (A) 7 is superposed so that the above air passage can be closed by heating the phosphor-containing photosensitive resin composition layer (A) 7.
- pressure can be reduced by putting the substrate 1 for PDP on which the phosphor-containing photosensitive resin composition layer (A) 7 is superposed, into a vacuum container horizontally, closing the vacuum container tightly and then exhausting air in the vacuum container.
- the shape of the vacuum container is not particularly limited, but from the point that property of embedding the phosphor-containing photosensitive resin composition layer (A) 7 in the space of the concave portion is further improved after the step of heating described below, it is preferred that the vacuum container has a heating apparatus for heating the substrate 1 for PDP on which the phosphor-containing photosensitive resin composition layer (A) 7 is superposed.
- the pressure in a vacuum container after reducing pressure is preferably 5 to 500 Pa, more preferably 10 to 200 Pa, particularly preferably 20 to 100 Pa. If the pressure is less than 5 Pa, exhaustion takes a long period of time so that operation efficiency tends to be lowered, while if it exceeds 500 Pa, property of embedding the phosphor-containing photosensitive resin composition layer (A) 7 in the space of the concave portion of the substrate 1 for PDP tends to be lowered.
- a heating method in the step of heating is not particularly limited, and there may be mentioned, for example, a method in which the substrate 1 for PDP is put on a heating apparatus such as a hot plate provided in a vacuum container and heating is carried out by heat transfer, and a method in which a light source of infrared ray is provided in a vacuum container and heating is carried out by radiation.
- the heating temperature is preferably 10 to 140 °C, more preferably 20 to 135 °C, particularly preferably 30 to 130 °C. If the heating temperature is lower than 10 °C, property of embedding the phosphor-containing photosensitive resin composition layer (A) 7 in the space of the concave portion of the substrate 1 for PDP tends to be lowered, while if it exceeds 140 °C, the phosphor-containing photosensitive resin composition layer (A) 7 tends to be thermoset.
- the heating time is preferably 1 hour or shorter, more preferably 20 minutes or shorter, particularly preferably 10 minutes or shorter. If the heating time exceeds 1 hour, the phosphor-containing photosensitive resin composition layer (A) 7 tends to be thermoset.
- the space 16 surrounded with the substrate 1 for PDP, the barrier rib 2 and the phosphor-containing photosensitive resin composition layer (A) 7 is in a tightly closed state.
- the pressure in the vacuum container can be returned to atmospheric pressure by, for example, introducing air or the like into the vacuum container.
- a time from starting to introduce air or the like into the vacuum container to returning the pressure to atmospheric pressure is preferably 30 minutes or shorter, more preferably 10 minutes or shorter, particularly preferably 5 minutes or shorter. If the time exceeds 30 minutes, property of embedding the phosphor-containing photosensitive resin composition layer (A) 7 in the space of the concave portion of the substrate 1 for PDP tends to be lowered.
- the phosphor-containing photosensitive resin composition layer (A) 7 can be adhered uniformly to the inner surface of the concave portion by using the adhesion method described above.
- a multicolor pattern comprising photosensitive resin composition layers each containing a phosphor which emits red, green or blue light is formed by repeating the respective steps of (Ie) to (IIIe) of the above process of the present invention for every color, the step of (IVe) is carried out to form a multicolor phosphor pattern.
- pattern formations of red, blue and green may be carried out in any order.
- a multicolor phosphor pattern which emit red, green and blue lights is formed by repeating the respective steps of (Ie) to (IVe) in the above process of the present invention for every color.
- Fig. 20 is a schematic drawing showing a plasma display panel for an alternating current in which the reference numeral 11 is a substrate (or a back plate glass substrate), 12 is a barrier rib, 13 is a discharge space, 14 is an electrode for address, 15 is a phosphor-containing photosensitive resin composition, 16 is a protective film, 17 is a dielectric material layer, 18 is a display electrode (a transparent electrode) and 19 is a front glass substrate.
- the front plate is the portion upper than the protective film 16 (inclusive) and the back plate is the portion not upper than the protective film 16 (exclusive).
- Fig. 20 an embodiment of applying the present invention to an alternating current plasma display panel is shown, but the composition of the present invention can be also applied to a plasma display panel for a direct current.
- a flask equipped with a stirrer, a reflux condenser, an inert gas-introducing inlet and a thermometer was charged with (1) shown in Table 1, and the temperature of the mixture was raised to 80 °C under nitrogen gas atmosphere. While maintaining the reaction temperature at 80 ⁇ 2 °C, (2) shown in Table 1 was uniformly added dropwise to the mixture over 4 hours.
- Film property-imparting polymer (a-1) having a weight average molecular weight of 80,000 and an acid value of 130 mgKOH/g.
- Material Formulation amount (1) Ethylene glycol monomethyl ether 70 parts by weight Toluene 50 parts by weight (2) Methacrylic acid 20 parts by weight Methyl methacrylate 55 parts by weight Ethyl acrylate 15 parts by weight n-Butyl methacrylate 10 parts by weight 2,2'-Azobis(isobutyronitrile) 0.5 part by weight
- a flask equipped with a stirrer, a reflux condenser, an inert gas-introducing inlet and a thermometer was charged with (1) shown in Table 2, and the temperature of the mixture was raised to 80 °C under nitrogen gas atmosphere. While maintaining the reaction temperature at 80 ⁇ 2 °C, (2) shown in Table 2 was uniformly added dropwise to the mixture over 4 hours.
- Ethylene glycol monomethyl ether 110 parts by weight Toluene 65 parts by weight (2) Methacrylic acid 50 parts by weight Methyl methacrylate 32 parts by weight Ethyl acrylate 18 parts by weight 2,2'-Azobis(isobutyronitrile) 2.2 parts by weight (3) Hydroquinone 0.05 part by weight (4) Glycidyl methacrylate 44.6 parts by weight Benzyltrimethylammonium chloride 0.1 part by weight Ethylene glycol monomethyl ether 60 parts by weight Toluene 60 parts by weight
- Material Formulation amount Film property-imparting polymer (a-2) obtained in Preparation example 2 131.58 parts by weight (60 parts by weight calculated on solid component)
- Polypropylene glycol dimethacrylate (the average number of propylene oxides: 12) 40 parts by weight 2-Benzyl-2-dimethylamino-1-(4-morpholinophenyl)-butanone-1 1 part by weight 1 part by weight (Y,Gd)BO 3 :Eu 210 parts by weight
- Binding agent (a low melting point glass) 3 parts by weight 3 parts by weight Methyl ethyl ketone 30 parts by weight
- Material Formulation amount Film property-imparting polymer (a-2) obtained in Preparation example 2 131.58 parts by weight (60 parts by weight calculated on solid component)
- Polypropylene glycol dimethacrylate (the average number of propylene oxides: 12) 40 parts by weight 2-Benzyl-2-dimethylamino-1-(4-morpholinophenyl)-butanone-1 1 part by weight BaMgAl 14 O 23 :Eu 2+ 160 parts by weight
- Solution (A-1) obtained in Preparation example 5 was coated uniformly on a polyethylene terephthalate film having a thickness of 20 ⁇ m and dried for 10 minutes by a hot air convection type dryer at 80 to 110 °C, and the solvent was removed to form a phosphor-containing photosensitive resin composition layer (A).
- the thickness after drying of the phosphor-containing photosensitive resin composition layer (A) obtained was 60 ⁇ m.
- edge fusion property is good (there is no exudation of the photosensitive layer even after 6 months)
- X edge fusion property is bad (exudation of the photosensitive layer occurs within 6 months)
- Photosensitive element (ii) was prepared.
- the thickness of the phosphor-containing photosensitive resin composition layer (A) of Photosensitive element (ii) was 60 ⁇ m.
- Photosensitive element (iii) was prepared.
- the thickness of the phosphor-containing photosensitive resin composition layer (A) of Photosensitive element (iii) was 60 ⁇ m.
- Photosensitive element (iv) was prepared.
- the thickness of the phosphor-containing photosensitive resin composition layer (A) of Photosensitive element (iv) was 60 ⁇ m.
- Photosensitive element (v) was prepared.
- the thickness of the phosphor-containing photosensitive resin composition layer (A) of Photosensitive element (v) was 60 ⁇ m.
- Photosensitive element (vi) was prepared.
- the thickness of the phosphor-containing photosensitive resin composition layer (A) of Photosensitive element (vi) was 60 ⁇ m.
- Photosensitive element (vii) was prepared.
- the thickness of the phosphor-containing photosensitive resin composition layer (A) of Photosensitive element (vii) was 60 ⁇ m.
- Photosensitive element (viii) was prepared.
- the thickness of the phosphor-containing photosensitive resin composition layer (A) of Photosensitive element (viii) was 60 ⁇ m.
- Photosensitive element (ix) was prepared.
- the thickness of the phosphor-containing photosensitive resin composition layer (A) of Photosensitive element (ix) was 60 ⁇ m.
- Photosensitive element (x) was prepared.
- the thickness of the phosphor-containing photosensitive resin composition layer (A) of Photosensitive element (x) was 60 ⁇ m.
- Photosensitive element (xi) was prepared.
- the thickness of the phosphor-containing photosensitive resin composition layer (A) of Photosensitive element (xi) was 60 ⁇ m.
- thermoplastic resin layer (B) was prepared.
- the thickness of the thermoplastic resin layer (B) of Film (xii) including the thermoplastic resin layer (B) was 70 ⁇ m.
- thermoplastic resin layer (B) was prepared.
- the thickness of the thermoplastic resin layer (B) of Film (xiii) including the thermoplastic resin layer (B) was 70 ⁇ m.
- thermoplastic resin layer (B) was prepared.
- the thickness of the thermoplastic resin layer (B) of Film (xiv) including the thermoplastic resin layer (B) was 70 ⁇ m.
- Example 2 In the same manner as in Example 1 except for changing Solution (A-1) for Phosphor-containing photosensitive resin composition layer (A) obtained in Preparation example 5 to Solution (C-1) for Embedding layer (C) obtained in Preparation example 20, Film (xv) including the embedding layer (C) was prepared.
- the thickness of the embedding layer (C) of Film (xv) including the embedding layer (C) was 34 ⁇ m.
- thermoplastic resin layer (B) obtained in Preparation example 17 was coated uniformly on a polyethylene terephthalate film having a thickness of 20 ⁇ m and dried for 10 minutes by a hot air convection type dryer at 80 to 110 °C, and distilled water was removed to form a thermoplastic resin layer (B).
- the thickness after drying of the thermoplastic resin layer (B) obtained was 70 ⁇ m.
- Solution (A-1) for Phosphor-containing photosensitive resin composition layer (A) obtained in Preparation example 5 was coated uniformly on the thermoplastic resin layer (B) and dried for 10 minutes by a hot air convection type dryer at 80 to 110 °C, and the solvent was removed to form a phosphor-containing photosensitive resin composition layer (A).
- the thickness of the phosphor-containing photosensitive resin composition layer (A) obtained was 60 ⁇ m.
- Photosensitive element (xvi) a polyethylene film having a thickness of 25 ⁇ m was pasted as a cover film to prepare Photosensitive element (xvi).
- Photosensitive element (xvii) was prepared.
- the thickness after drying of the thermoplastic resin layer (B) of Photosensitive element (xvii) was 70 ⁇ m, and the thickness of the phosphor-containing photosensitive resin composition layer (A) was 60 ⁇ m.
- Photosensitive element (xviii) was prepared.
- the thickness after drying of the thermoplastic resin layer (B) of Photosensitive element (xviii) was 70 ⁇ m, and the thickness of the phosphor-containing photosensitive resin composition layer (A) was 60 ⁇ m.
- Photosensitive element (xx) was prepared.
- the thickness after drying of the thermoplastic resin layer (B) of Photosensitive element (xx) was 70 ⁇ m, and the thickness of the phosphor-containing photosensitive resin composition layer (A) was 60 ⁇ m.
- Photosensitive element (xxi) was prepared.
- the thickness after drying of the thermoplastic resin layer (B) of Photosensitive element (xxi) was 70 ⁇ m, and the thickness of the phosphor-containing photosensitive resin composition layer (A) was 60 ⁇ m.
- Photosensitive element (xxii) having a thickness after drying of the thermoplastic resin layer (B) being 43 ⁇ m was prepared.
- the thickness of the phosphor-containing photosensitive resin composition layer (A) of Photosensitive element (xxii) was 60 ⁇ m which was the same as in Example 1.
- Photosensitive element (xxiii) was prepared.
- the thickness after drying of the embedding layer (C) of Photosensitive element (xxiii) was 70 ⁇ m, and the thickness of the phosphor-containing photosensitive resin composition layer (A) was 60 ⁇ m.
- Photosensitive element (xxvii) was prepared.
- the thickness of the phosphor-containing photosensitive resin composition layer (A) of Photosensitive element (xxvii) was 60 ⁇ m.
- Photosensitive element (xxviii) was prepared.
- the thickness after drying of the embedding layer (C) of Photosensitive element (xxviii) was 70 ⁇ m, and the thickness of the phosphor-containing photosensitive resin composition layer (A) was 60 ⁇ m.
- Photosensitive element (xxix) was prepared.
- the thickness after drying of the embedding layer (C) of Photosensitive element (xxix) was 70 ⁇ m, and the thickness of the phosphor-containing photosensitive resin composition layer (A) was 60 ⁇ m.
- Photosensitive element (xxiv) was prepared.
- the thickness of the phosphor-containing photosensitive resin composition layer (A) of Photosensitive element (xxiv) was 60 ⁇ m.
- thermoplastic resin layer (B) Step of heating and pressurizing the thermoplastic resin layer (B) in a state that the thermoplastic resin layer (B) is superposed on the phosphor-containing photosensitive resin composition layer (A) on an uneven surface of a substrate having unevenness, to laminate the phosphor-containing photosensitive resin composition layer (A) and the thermoplastic resin layer (B) on the uneven surface>
- Photosensitive element (i) including the phosphor-containing photosensitive resin composition layer (A) obtained in Example 1 was laminated by using a vacuum laminator (trade name: VLM-1 Model, produced by Hitachi Chemical Co., Ltd.) at a heat shoe temperature of 30 °C and a lamination rate of 1.5 m/min under an atmospheric pressure of 4,000 Pa or less and a contact bonding pressure (cylinder pressure) of 5 x 10 4 Pa (since a substrate having a thickness of 3 mm, a length of 10 cm and a width-of 10 cm (a square) was used, line pressure at this time was 2.4 x 10 3 N/m) while the polyethylene film of Photosensitive element (i) was peeled off.
- a vacuum laminator trade name: VLM-1 Model, produced by Hitachi Chemical Co., Ltd.
- the polyethylene terephthalate film of Photosensitive ) element (i) including the phosphor-containing photosensitive resin composition layer (A) was peeled off.
- Film (xii) including the thermoplastic resin layer (B) obtained in Example 12 was laminated by using a laminator (trade name: HLM-3000 Model, produced by Hitachi Chemical Co., Ltd.) at a lamination temperature of 110 °C and a lamination rate of 0.5 m/min under a contact bonding pressure (cylinder pressure) of 4 x 10 5 Pa (since a substrate having a thickness of 3 mm, a length of 10 cm and a width of 10 cm (a square) was used, line pressure at this time was 9.8 x 10 3 N/m) while the polyethylene film of Film (xii) was peeled off.
- a laminator trade name: HLM-3000 Model, produced by Hitachi Chemical Co., Ltd.
- the substrate was left to stand at ordinary temperature for 1 hour and then subjected to spray development at 30 °C for 70 seconds by using a 1 % by weight sodium carbonate aqueous solution.
- the substrate was dried at 80 °C for 10 minutes, and by using a Toshiba UV ray irradiation apparatus produced by Toshiba Denzai Co., Japan, 3 J/cm 2 of UV ray was irradiated.
- heating treatment was carried out at 550 °C for 30 minutes to remove unnecessary resin components, whereby a phosphor pattern was formed in the space of the substrate for PDP.
- the section of the phosphor pattern obtained was observed visually by a stereoscopic microscope and SEM to evaluate the formation state of the phosphor pattern.
- the results are shown in Table 21.
- the standard of evaluation is shown below.
- a phosphor layer is formed uniformly in the space (on the wall surface of a barrier rib and the bottom of a cell) of a substrate for PDP
- a phosphor layer is not formed uniformly in the space (on the wall surface of a barrier rib and the bottom of a cell) of a substrate for PDP
- the ratio (V 1 )/(V 2 ) of the total volume (V 1 ) of the phosphor-containing photosensitive resin composition layer (A) and the thermoplastic resin layer (B) to the volume (V 2 ) of the space of the concave portion of the substrate for PDP was determined, and the results are shown in Table 21.
- Example 27 In the same manner as in Example 27 except for changing Film (xii) including the thermoplastic resin layer (B) to Film (xiii) including the thermoplastic resin layer (B) obtained in Example 13, a phosphor pattern was formed, the formation state of the phosphor pattern obtained was evaluated, and (x)/(y) and (V 1 )/(V 2 ) thereof were determined. The results are shown in Table 21.
- Example 21 In the same manner as in Example 27 except for changing Film (xii) including the thermoplastic resin layer (B) to Film (xiv) including the thermoplastic resin layer (B) obtained in Example 14, a phosphor pattern was formed, the formation state of the phosphor pattern obtained was evaluated, and (x)/(y) and (V 1 )/(V 2 ) thereof were determined. The results are shown in Table 21.
- the substrate was developed by using a 1 % by weight sodium carbonate aqueous solution, it was further developed by using an aqueous solution containing 5 % by weight of borax and 20 % by weight of butylcarbitol.
- Example 27 In the same manner as in Example 27 except for changing Photosensitive element (i) including the phosphor-containing photosensitive resin composition layer (A) to Photosensitive element (x) including the phosphor-containing photosensitive resin composition layer (A) obtained in Example 10 and changing Film (xii) including the thermoplastic resin layer (B) to Film (xiii) including the thermoplastic resin layer (B) obtained in Example 13, a phosphor pattern was formed, the formation state of the phosphor pattern obtained was evaluated, and (x)/(y) and (V 1 )/(V 2 ) thereof were determined. The results are shown in Table 21.
- Example 27 In the same manner as in Example 27 except for changing Photosensitive element (i) including the phosphor-containing photosensitive resin composition layer (A) to Photosensitive element (xi) including the phosphor-containing photosensitive resin composition layer (A) obtained in Example 11 and changing Film (xii) including the thermoplastic resin layer (B) to Film (xiii) including the thermoplastic resin layer (B) obtained in Example 13, a phosphor pattern was formed, the formation state of the phosphor pattern obtained was evaluated, and (x)/(y) and (V 1 )/(V 2 ) thereof were determined. The results are shown in Table 21.
- Photosensitive element (ii) obtained in Example 2 was laminated by using a vacuum laminator (trade name: VLM-1 Model, produced by Hitachi Chemical Co., Ltd.) at a heat shoe temperature of 30 °C and a lamination rate of 1.5 m/min under an atmospheric pressure of 4,000 Pa or less and a contact bonding pressure (cylinder pressure) of 5 x 10 4 Pa (since a substrate having a thickness of 3 mm, a length of 10 cm and a width of 10 cm (a square) was used, line pressure at this time was 2.4 x 10 3 N/m) while the polyethylene film of Photosensitive element (ii) was peeled off.
- a vacuum laminator trade name: VLM-1 Model, produced by Hitachi Chemical Co., Ltd.
- the substrate was left to stand at ordinary temperature for 1 hour and then subjected to spray development at 30 °C for 70 seconds by using a 1 % by weight sodium carbonate aqueous solution.
- the substrate was dried at 80°C for 10 minutes, and by using a Toshiba UV ray irradiation apparatus produced by Toshiba Denzai Co., Japan, 3 J/cm 2 of UV ray was irradiated.
- heating treatment was carried out at 550 °C for 30 minutes to remove unnecessary resin components, whereby a phosphor pattern was formed in the space of the substrate for PDP.
- Example 45 In the same manner as in Example 45 except for changing the embedding layer (C) of the polyethylene film (xxv) (Vicat softening point: 82 to 100 °C) having a film thickness of 100 ⁇ m in the step (Ic) to the embedding layer (C) of a polypropylene film (xxvi) (Vicat softening point: 125 to 155 °C) having a film thickness of 100 ⁇ m, a phosphor pattern was formed. In the same manner as in Example 27, the formation state of the phosphor pattern obtained was evaluated, and (x)/(y) and (V' 1 )/(V' 2 ) thereof were determined. The results are shown in Table 21.
- Example 45 In the same manner as in Example 45 except for changing the step (Ic) and the step (IIc) as shown below, a phosphor pattern was formed. In the same manner as in Example 27, the formation state of the phosphor pattern obtained was evaluated, and (x)/(y) and (V' 1 )/(V' 2 ) thereof were determined. The results are shown in Table 21.
- Photosensitive element (ii) obtained in Example 2 was laminated by using a laminator (trade name: HLM-3000 Model, produced by Hitachi Chemical Co., Ltd.) at a lamination temperature of 60 °C and a lamination rate of 0.5 m/min under a contact bonding pressure (cylinder pressure) of 5 x 10 4 Pa (since a substrate having a thickness of 3 mm, a length of 10 cm and a width of 10 cm (a square) was used, line pressure at this time was 2.4 x 10 3 N/m) while the polyethylene film of Photosensitive element (ii) was peeled off.
- a laminator trade name: HLM-3000 Model, produced by Hitachi Chemical Co., Ltd.
- ⁇ (Ib) Step of heating and pressurizing a photosensitive element having a support film, the thermoplastic resin layer (B) provided on the support film and the phosphor-containing photosensitive resin composition layer (A) provided thereon so that the phosphor-containing photosensitive resin composition layer (A) is contacted with an uneven surface of a substrate having unevenness, to laminate the phosphor-containing photosensitive resin composition layer (A) and the thermoplastic resin-layer (B) on the uneven surface>
- Photosensitive element (xvi) obtained in Example 16 was laminated by using a vacuum laminator (trade name: VLM-1 Model, produced by Hitachi Chemical Co., Ltd.) at a heat shoe temperature of 110 °C and a lamination rate of 0.5 m/min under an atmospheric pressure of 4,000 Pa or less and a contact bonding pressure (cylinder pressure) of 4 x 10 5 Pa (since a substrate having a thickness of 3 mm, a length of 10 cm and a width of 10 cm (a square) was used, line pressure at this time was 9.8 x 10 3 N/m) while the polyethylene film of Photosensitive element (xvi) was peeled off.
- a vacuum laminator trade name: VLM-1 Model, produced by Hitachi Chemical Co., Ltd.
- the substrate was left to stand at ordinary temperature for 1 hour and then subjected to spray development at 30 °C for 70 seconds by using a 1 % by weight sodium carbonate aqueous solution. After development, the substrate was dried at 80 °C for 10 minutes, and by using a Toshiba UV ray irradiation apparatus produced by Toshiba Denzai Co., Japan, 3 J/cm 2 of UV ray was irradiated.
- heating treatment was carried out at 550 °C for 30 minutes to remove unnecessary resin components, whereby a phosphor pattern was formed in the space of the substrate for PDP.
- Example 27 In the same manner as in Example 48 except for changing Photosensitive element (xvi) obtained in Example 16 to Photosensitive element (xvii) obtained in Example 17, a phosphor pattern was formed. In the same manner as in Example 27, the formation state of the phosphor pattern obtained was evaluated, and (x)/(y) and (V 1 )/(V 2 ) thereof were determined. The results are shown in Table 21.
- Example 48 In the same manner as in Example 48 except for changing Photosensitive element (xvi) obtained in Example 16 to Photosensitive element (xviii) obtained in Example 18, a phosphor pattern was formed. In the same manner as in Example 27, the formation state of the phosphor pattern obtained was evaluated, and (x)/(y) and (V 1 )/(V 2 ) thereof were determined. The results are shown in Table 21.
- Example 48 In the same manner as in Example 48 except for changing Photosensitive element (xvi) obtained in Example 16 to Photosensitive element (xix) obtained in Example 19, a phosphor pattern was formed. In the same manner as in Example 27, the formation state of the phosphor pattern obtained was evaluated, and (x)/(y) and (V 1 )/(V 2 ) thereof were determined. The results are shown in Table 21.
- Example 48 In the same manner as in Example 48 except for changing Photosensitive element (xvi) obtained in Example 16 to Photosensitive element (xx) obtained in Example 20, a phosphor pattern was formed. In the same manner as in Example 27, the formation state of the phosphor pattern obtained was evaluated, and (x)/(y) and (V 1 )/(V 2 ) thereof were determined. The results are shown in Table 21.
- Example 48 In the same manner as in Example 48 except for changing Photosensitive element (xvi) obtained in Example 16 to Photosensitive element (xxi) obtained in Example 21 and changing ⁇ (IIIb) Step of removing unnecessary portions from the phosphor-containing photosensitive resin composition layer (A) and/or the thermoplastic resin layer (B) by development> as shown below, a phosphor pattern was formed. In the same manner as in Example 27, the formation state of the phosphor pattern obtained was evaluated, and (x)/(y) and (V 1 )/(V 2 ) thereof were determined. The results are shown in Table 21.
- the substrate was developed by using a 1 % by weight sodium carbonate aqueous solution, it was further developed by using an aqueous solution containing 5 % by weight of borax and 20 % by weight of butylcarbitol.
- Example 48 In the same manner as in Example 48 except for changing ⁇ (Ib) Step of heating and pressurizing a photosensitive element having a support film, the thermoplastic resin layer (B) provided on the support film and the phosphor-containing photosensitive resin composition layer (A) provided thereon so that the phosphor-containing photosensitive resin composition layer (A) is contacted with an uneven surface of a substrate having unevenness, to laminate the phosphor-containing photosensitive resin composition layer (A) and the thermoplastic resin layer (B) on the uneven surface> as shown below, a phosphor pattern was formed.
- Example 27 the formation state of the phosphor pattern obtained was evaluated, and (x)/(y) and (V 1 )/(V 2 ) thereof were determined. The results are shown in Table 21.
- ⁇ (Ib) Step of heating and pressurizing a photosensitive element having a support film, the thermoplastic resin layer (B) provided on the support film and the phosphor-containing photosensitive resin composition layer (A) provided thereon so that the phosphor-containing photosensitive resin composition layer (A) is contacted with an uneven surface of a substrate having unevenness, to laminate the phosphor-containing photosensitive resin composition layer (A) and the thermoplastic resin layer (B) on the uneven surface>
- a substrate of PDP (having a striped barrier rib, opening width of barrier rib: 150 ⁇ m, width of barrier rib: 70 ⁇ m, height of barrier rib: 150 ⁇ m) was heated by a hot plate at 80 °C for 5 minutes.
- Photosensitive element (xxii) obtained in Example 22 was laminated by using a laminator (trade name: HLM-1500 Model, produced by Hitachi Chemical Co., Ltd.) at a lamination temperature of 110 °C and a lamination rate of 0.2 m/min under a contact bonding pressure of 4 x 10 5 Pa (since a substrate having a thickness of 3 mm, a length of 10 cm and a width of 10 cm (a square) was used, line pressure at this time was 9.8 x 10 3 N/m) while the polyethylene film of Photosensitive element (xxii) was peeled off.
- a laminator trade name: HLM-1500 Model, produced by Hitachi Chemical Co., Ltd.
- Photosensitive element (xxiii) obtained in Example 23 was laminated by using a vacuum laminator (trade name: VLM-1 Model, produced by Hitachi Chemical Co., Ltd.) at a heat shoe temperature of 110 °C and a lamination rate of 0.5 m/min under an atmospheric pressure of 4,000 Pa or less and a contact bonding pressure (cylinder pressure) of 4 x 10 5 Pa (since a substrate having a thickness of 3 mm, a length of 10 cm and a width of 10 cm (a square) was used, line pressure at this time was 9.8 x 10 3 N/m) while the polyethylene film of Photosensitive element (xxiii) was peeled off.
- a vacuum laminator trade name: VLM-1 Model, produced by Hitachi Chemical Co., Ltd.
- the substrate was left to stand at ordinary temperature for 1 hour and then subjected to spray development at 30 °C for 70 seconds by using a 1 % by weight sodium carbonate aqueous solution.
- the substrate was dried at 80 °C for 10 minutes, and by using a Toshiba UV ray irradiation apparatus produced by Toshiba Denzai Co., Japan, 3 J/cm 2 of UV ray was irradiated.
- heating treatment was carried out at 550 °C for 30 minutes to remove unnecessary resin components, whereby a phosphor pattern was formed in the space of the substrate for PDP.
- Photosensitive element (i) obtained in Example 1 was laminated by using a vacuum laminator (trade name: VLM-1 Model, produced by Hitachi Chemical Co., Ltd.) at a heat shoe temperature of 110 °C and a lamination rate of 0.5 m/min under atmospheric pressure and a contact bonding pressure (cylinder pressure) of 1 x 10 4 Pa (since a substrate having a thickness of 3 mm, a length of 10 cm and a width of 10 cm (a square) was used, line pressure at this time was 4.8 x 10 2 N/m) while the polyethylene film of Photosensitive element (i) was peeled off.
- a vacuum laminator trade name: VLM-1 Model, produced by Hitachi Chemical Co., Ltd.
- the substrate was left to stand at ordinary temperature for 1 hour and then subjected to spray development at 30 °C for 70 seconds by using a 1 % by weight sodium carbonate aqueous solution. After development, the substrate was dried at 80 °C for 10 minutes, and by using a Toshiba UV ray irradiation apparatus produced by Toshiba Denzai Co., Japan, 3 J/cm 2 of UV ray was irradiated.
- heating treatment was carried out at 550 °C for 30 minutes to remove unnecessary resin components, whereby a phosphor pattern was formed in the space of the substrate for PDP.
- Example 56 In the same manner as in Example 56 except for changing the step (Ie) shown below, a phosphor pattern was formed. In the same manner as in Example 27, the formation state of the phosphor pattern obtained was evaluated, and (x)/(y) thereof was determined. The results are shown in Table 21.
- Photosensitive element (vi) was superposed at a side on which a lattice-shaped barrier rib (opening width of barrier rib: 250 x 350 ⁇ m, width of barrier rib: 50 ⁇ m, height of barrier rib: 150 ⁇ m) was formed, of a substrate for PDP on which the barrier rib was formed in a region of 121.9 x 162.6 mm in the center of a glass plate having a size of 200 x 200 x 3 mm so that the phosphor-containing photosensitive resin composition layer (A) is contacted with the barrier rib and the periphery of the region where the barrier rib was formed was covered with a width of 1 cm or more of Photosensitive element (vi).
- a lattice-shaped barrier rib opening width of barrier rib: 250 x 350 ⁇ m, width of barrier rib: 50 ⁇ m, height of barrier rib: 150 ⁇ m
- the polyethylene terephthalate film existing on the phosphor-containing photosensitive resin composition layer (A) superposed on the substrate for PDP was peeled off, the substrate was placed in a vacuum dryer equipped with a heating apparatus, and pressure was reduced to 80 Pa at ordinary temperature.
- Example 56 In the same manner as in Example 56 except for using a roll having a surface made of a sponge and moving the roll in a direction parallel to the rib to apply a pressure of 2 x 10 5 Pa in terms of gauge pressure (ordinary pressure 1 atm is 0) in the step (Ie), the phosphor-containing photosensitive resin composition layer (A) was adhere to the inner surface of the concave portion, whereby a phosphor pattern was formed in the space of the substrate for PDP. In the same manner as in Example 27, the formation state of the phosphor pattern obtained was evaluated, and (x)/(y) thereof was determined. The results are shown in Table 21.
- Example 27 In the same manner as in Example 28 except for changing Photosensitive element (i) including the phosphor-containing photosensitive resin composition layer (A) to Photosensitive element (xxvii) including the phosphor-containing photosensitive resin composition layer (A) obtained in Example 24 and changing ⁇ (IIIa) Step of removing unnecessary portions from the phosphor-containing photosensitive resin composition layer (A) and/or the thermoplastic resin layer (B) by development> as shown below, a phosphor pattern was formed. In the same manner as in Example 27, the formation state of the phosphor pattern obtained was evaluated, and (x)/(y) and (V 1 )/(V 2 ) thereof were determined. The results are shown in Table 21.
- the substrate was dried at 80 °C for 10 minutes, and by using a Toshiba UV ray irradiation apparatus produced by Toshiba Denzai Co., Japan, 3 J/cm 2 of UV ray was irradiated.
- Example 47 In the same manner as in Example 47 except for changing Photosensitive element (ii) including the phosphor-containing photosensitive resin composition layer (A) to Photosensitive element (xxvii) including the phosphor-containing photosensitive resin composition layer (A) obtained in Example 24 and changing ⁇ (IVc) Step of removing an unnecessary portion from the phosphor-containing photosensitive resin composition layer (A) by development> as shown below, a phosphor pattern was formed. In the same manner as in Example 27, the formation state of the phosphor pattern obtained was evaluated, and (x)/(y) and (V' 1 )/(V' 2 ) thereof were determined. The results are shown in Table 21.
- the substrate was dried at 80 °C for 10 minutes, and by using a Toshiba UV ray irradiation apparatus produced by Toshiba Denzai Co., Japan, 3 J/cm 2 of UV ray was irradiated.
- Example 27 In the same manner as in Example 27 except for changing ⁇ (IIIa) Step of removing unnecessary portions from the phosphor-containing photosensitive resin composition layer (A) and/or the thermoplastic resin layer (B) by development> as shown below, a phosphor pattern was formed, the formation state of the phosphor pattern obtained was evaluated, and (x)/(y) and (V 1 )/(V 2 ) thereof were determined. The results are shown in Table 21.
- the substrate was left to stand at ordinary temperature for 1 hour and then subjected to spray development at 30 °C for 70 seconds by using a 1 % by weight sodium carbonate aqueous solution.
- the substrate was dried at 80 °C for 10 minutes, and by using a Toshiba UV ray irradiation apparatus produced by Toshiba Denzai Co., Japan, 3 J/cm 2 of UV ray was irradiated.
- Example 27 In the same manner as in Example 27 except for changing ⁇ (IIa) Step of irradiating the phosphor-containing photosensitive resin composition layer (A) and/or the thermoplastic resin layer (B) imagewisely with active light> as shown below, a phosphor pattern was formed, the formation state of the phosphor pattern obtained was evaluated, and (x)/(y) and (V 1 )/(V 2 ) thereof were determined. The results are shown in Table 21.
- a photomask having an active light permeation width (130 ⁇ m) which was narrower by 20 ⁇ m than the opening width 150 ⁇ m of the barrier rib was adhered to the polyethylene terephthalate film of Film (xii) including the thermoplastic resin layer (B) so that the center of the active light permeation width of the photomask was positioned at the center of the opening width of the barrier rib.
- a HMW-201GX Model exposer (trade name) produced by Orc Seisakusho Co., Japan, 100 mJ/cm 2 of active light was irradiated imagewisely.
- Example 21 In the same manner as in Example 55 except for changing Photosensitive element (xxiii) obtained in Example 23 to Photosensitive element (xxviii) obtained in Example 25, a phosphor pattern was formed. In the same manner as in Example 27, the formation state of the phosphor pattern obtained was evaluated, and (x)/(y) thereof was determined. The results are shown in Table 21.
- Example 21 In the same manner as in Example 55 except for changing Photosensitive element (xxiii) obtained in Example 23 to Photosensitive element (xxix) obtained in Example 26, a phosphor pattern was formed. In the same manner as in Example 27, the formation state of the phosphor pattern obtained was evaluated, and (x)/(y) thereof was determined. The results are shown in Table 21.
- Example 21 In the same manner as in Example 27 except for not using Film (xii) including the thermoplastic resin layer (B), a phosphor pattern was formed, the formation state of the phosphor pattern obtained was evaluated. The results are shown in Table 21.
- Example 21 In the same manner as in Example 31 except for not using Film (xiv) including the thermoplastic resin layer (B), a phosphor pattern was formed. In the same manner as in Example 27, the formation state of the phosphor pattern obtained was evaluated. The results are shown in Table 21.
- Example 21 In the same manner as in Example 32 except for not using Film (xiv) including the thermoplastic resin layer (B), a phosphor pattern was formed. In the same manner as in Example 27, the formation state of the phosphor pattern obtained was evaluated. The results are shown in Table 21.
- Example 33 In the same manner as in Example 33 except for not using Film (xii) including the thermoplastic resin layer (B), a phosphor pattern was formed. In the same manner as in Example 27, the formation state of the phosphor pattern obtained was evaluated. The results are shown in Table 21.
- Example 27 In the same manner as in Example 36 except for not using Film (xii) including the thermoplastic resin layer (B), a phosphor pattern was formed. In the same manner as in Example 27, the formation state of the phosphor pattern obtained was evaluated. The results are shown in Table 21.
- Example 27 In the same manner as in Example 38 except for not using Film (xii) including the thermoplastic resin layer- (B), a phosphor pattern was formed. In the same manner as in Example 27, the formation state of the phosphor pattern obtained was evaluated. The results are shown in Table 21.
- Example 21 In the same manner as in Example 40 except for not using Film (xii) including the thermoplastic resin layer (B), a phosphor pattern was formed. In the same manner as in Example 27, the formation state of the phosphor pattern obtained was evaluated. The results are shown in Table 21.
- Example 21 In the same manner as in Example 42 except for not using Film (xiii) including the thermoplastic resin layer (B), a phosphor pattern was formed. In the same manner as in Example 27, the formation state of the phosphor pattern obtained was evaluated. The results are shown in Table 21.
- Example 44 In the same manner as in Example 44 except for not using Film (xiii) including the thermoplastic resin layer (B), a phosphor pattern was formed. In the same manner as in Example 27, the formation state of the phosphor pattern obtained was evaluated. The results are shown in Table 21.
- the substrate on which the photosensitive resin composition layer containing the phosphor emitting red light (first color) was formed obtained by carrying out the steps of (Ia) to (IIIa) in Example 36, the steps of (Ia) to (IIIa) in Example 38 were carried out to form a photosensitive resin composition layer containing a phosphor emitting blue light (second color), and then the steps of (Ia) to (IIIa) in Example 40 were carried out to form a photosensitive resin composition layer containing a phosphor emitting green light (third color), whereby a multicolor pattern was prepared.
- the section of the multicolor phosphor pattern emitting red, green and blue lights obtained was observed visually by a stereoscopic microscope and SEM to evaluate the formation state of the multicolor phosphor pattern.
- the results are shown in Table 22.
- the standard of evaluation is shown below.
- a multicolor phosphor layer emitting red, green and blue lights is formed uniformly in the space (on the wall surface of a barrier rib and the bottom of a cell) of a substrate for PDP
- X a multicolor phosphor layer emitting red, green and blue lights is not formed uniformly in the space (on the wall surface of a barrier rib and the bottom of a cell) of a substrate for PDP
- the substrate on which the photosensitive resin composition layer containing the phosphor emitting red light (first color) was formed obtained by carrying out the steps of (Ib) to (IIIb) in Example 49, the steps of (Ib) to (IIIb) in Example 51 were carried out to form a photosensitive resin composition layer containing a phosphor emitting blue light (second color), and then the steps of (Ib) to (IIIb) in Example 52 were carried out to form a photosensitive resin composition layer containing a phosphor emitting green light (third color), whereby a multicolor pattern was obtained to prepare a back plate.
- Example 69 In the same manner as in Example 69, the formation state of the multicolor phosphor pattern obtained was evaluated. The results are shown in Table 22.
- the substrate on which the photosensitive resin composition layer containing the phosphor emitting red light (first color) was formed obtained by carrying out the steps of (Ic) to (IVc) in Example 47, the steps of (Ic) to (IVc) in Example 63 were carried out to form a photosensitive resin composition layer containing a phosphor emitting blue light (second color), and then the steps of (Ic) to (IVc) in Example 64 were carried out to form a photosensitive resin composition layer containing a phosphor emitting green light (third color), whereby a multicolor pattern was obtained to prepare a back plate.
- Example 69 In the same manner as in Example 69, the formation state of the multicolor phosphor pattern obtained was evaluated. The results are shown in Table 22.
- the substrate on which the photosensitive resin composition layer containing the phosphor emitting red light (first color) was formed obtained by carrying out the steps of (Id) to (IVd) in Example 55, the steps of (Id) to (IVd) in Example 67 were carried out to form a photosensitive resin composition layer containing a phosphor emitting blue light (second color), and then the steps of (Id) to (IVd) in Example 68 were carried out to form a photosensitive resin composition layer containing a phosphor emitting green light (third color), whereby a multicolor pattern was obtained to prepare a back plate.
- Example 69 In the same manner as in Example 69, the formation state of the multicolor phosphor pattern obtained was evaluated. The results are shown in Table 22.
- the substrate on which the photosensitive resin composition layer containing the phosphor emitting red light (first color) was formed obtained by carrying out the steps of (Ie) to (IIIe) in Example 57, the steps of (Ie) to (IIIe) in Example 65 were carried out to form a photosensitive resin composition layer containing a phosphor emitting blue light (second color), and then the steps of (Ie) to (IIIe) in Example 66 were carried out to form a photosensitive resin composition layer containing a phosphor emitting green light (third color), whereby a multicolor pattern was obtained to prepare a back plate.
- Example 66 the step of (IVe) in Example 66 was carried out to prepare a multicolor phosphor pattern.
- Example 69 In the same manner as in Example 69, the formation state of the multicolor phosphor pattern obtained was evaluated. The results are shown in Table 22.
- the substrate on which the photosensitive resin composition layer containing the phosphor emitting red light (first color) was formed obtained by carrying out the steps of (Ia) to (IIIa) in Example 36 in the same manner except for changing the step (IIIa) as shown below, the steps of (Ia) to (IIIa) in Example 38 were carried out in the same manner except for changing the step (IIIa) as shown below to form a photosensitive resin composition layer containing a phosphor emitting blue light (second color), and then the steps of (Ia) to (IIIa) in Example 40 were carried out in the same manner except for changing the step (IIIa) as shown below to form a photosensitive resin composition layer containing a phosphor emitting green light (third color), whereby a multicolor pattern was obtained to prepare a back plate.
- the substrate was left to stand at ordinary temperature for 1 hour and then subjected to spray development at 30 °C for 100 seconds by using a 1 % by weight sodium carbonate aqueous solution. After development, the substrate was dried at 80 °C for 10 minutes, and by using a Toshiba UV ray irradiation apparatus produced by Toshiba Denzai Co., Japan, 3 J/cm 2 of UV ray was irradiated.
- Example 69 In the same manner as in Example 69, the formation state of the multicolor phosphor pattern obtained was evaluated. The results are shown in Table 22.
- the substrate on which the photosensitive resin composition layer containing the phosphor emitting red light (first color) was formed obtained by carrying out the steps of (Ia) to (IVa) in Example 36, the steps of (Ia) to (IVa) in Example 38 were carried out to form a photosensitive resin composition layer containing a phosphor emitting blue light (second color), and then the steps of (Ia) to (IVa) in Example 40 were carried out to form a photosensitive resin composition layer containing a phosphor emitting green light (third color), whereby a multicolor phosphor pattern was obtained to prepare a back plate.
- Example 69 In the same manner as in Example 69, the formation state of the multicolor phosphor pattern obtained was evaluated. The results are shown in Table 22.
- the substrate on which the photosensitive resin composition layer containing the phosphor emitting red light (first color) was formed obtained by carrying out the steps of (Ib) to (IVb) in Example 49, the steps of (Ib) to (IVb) in Example 51 were carried out to form a photosensitive resin composition layer containing a phosphor emitting blue light (second color), and then the steps of (Ib) to (IVb) in Example 52 were carried out to form a photosensitive resin composition layer containing a phosphor emitting green light (third color), whereby a multicolor phosphor pattern was obtained to prepare a back plate.
- Example 69 In the same manner as in Example 69, the formation state of the multicolor phosphor pattern obtained was evaluated. The results are shown in Table 22.
- the substrate on which the photosensitive resin composition layer containing the phosphor emitting red light (first color) was formed obtained by carrying out the steps of (Ic) to (Vc) in Example 47, the steps of (Ic) to (Vc) in Example 63 were carried out to form a photosensitive resin composition layer containing a phosphor emitting blue light (second color), and then the steps of (Ic) to (Vc) in Example 64 were carried out to form a photosensitive resin composition layer containing a phosphor emitting green light (third color), whereby a multicolor phosphor pattern was obtained to prepare a back plate.
- Example 69 In the same manner as in Example 69, the formation state of the multicolor phosphor pattern obtained was evaluated. The results are shown in Table 22.
- the substrate on which the photosensitive resin composition layer containing the phosphor emitting red light (first color) was formed obtained by carrying out the steps of (Id) to (Vd) in Example 55, the steps of (Id) to (Vd) in Example 67 were carried out to form a photosensitive resin composition layer containing a phosphor emitting blue light (second color), and then the steps of (Id) to (Vd) in Example 68 were carried out to form a photosensitive resin composition layer containing a phosphor emitting green light (third color), whereby a multicolor phosphor pattern was obtained to prepare a back plate.
- Example 69 In the same manner as in Example 69, the formation state of the multicolor phosphor pattern obtained was evaluated. The results are shown in Table 22.
- the substrate on which the photosensitive resin composition layer containing the phosphor emitting red light (first color) was formed obtained by carrying out the steps of (Ie) to (IVe) in Example 57, the steps of (Ie) to (IVe) in Example 65 were carried out to form a photosensitive resin composition layer containing a phosphor emitting blue light (second color), and then the steps of (Ie) to (IVe) in Example 66 were carried out to form a photosensitive resin composition layer containing a phosphor emitting green light (third color), whereby a multicolor phosphor pattern was obtained to prepare a back plate.
- Example 69 O
- Example 70 O
- Example 71 O
- Example 72 O
- Example 73 O
- Example 74 O
- Example 75 O
- Example 76 O
- Example 77 O
- Example 78 O
- Example 79 O
- the photosensitive elements of the present invention have good edge fusion property, and in the process for preparing a phosphor pattern of the present invention using the thermoplastic resin layer (B), the embedding layer (C) or various pressures, phosphor pattern-forming property (property of embedding on the wall surface of a barrier rib and the bottom of a space of a substrate for PDP) is also good.
- thermoplastic resin layer (B) the embedding layer (C) nor various pressures, phosphor pattern-forming property (property of embedding on the wall surface of a barrier rib and the bottom of a space of a substrate for PDP) is poor.
- the invention according to Claim 1 can suppress lowering of apparent luminance in visual recognition from a wide angle of a field of view in a phosphor pattern of PDP.
- the invention according to Claim 2 has excellent property of embedding in a space of a substrate having unevenness such as a substrate for PDP (property of forming a phosphor-containing photosensitive resin composition layer on the wall surface of a barrier rib and the bottom of a space of a substrate for PDP) and can form a phosphor pattern with high precision and a uniform shape.
- a substrate for PDP property of forming a phosphor-containing photosensitive resin composition layer on the wall surface of a barrier rib and the bottom of a space of a substrate for PDP
- the invention according to Claim 3 has excellent operatability in addition to the effects of the invention according to Claim 2.
- the invention according to Claim 4 has excellent property of suppressing decrease in phosphor-containing photosensitive resin composition layer thickness in addition to the effects of the invention according to Claim 2 or 3.
- the invention according to Claim 10 has excellent property of suppressing edge fusion and property of embedding in a space of a substrate having unevenness such as a substrate for PDP and can form a phosphor pattern with high precision and a uniform shape with good operatability.
- the invention according to Claim 15 has excellent operatability, environmental safety and property of embedding in a space of a substrate having unevenness such as a substrate for PDP and can form a phosphor pattern with high precision and a uniform shape.
- the invention according to Claim 16 has more excellent operatability in addition to the effects of the invention according to Claim 15.
- the invention according to Claim 17 has excellent property of suppressing decrease in phosphor-containing photosensitive resin composition layer thickness in addition to the effects of the invention according to Claim 15 or 16.
- the invention according to Claim 23 has excellent property of embedding in a space of a substrate having unevenness such as a substrate for PDP and can form a phosphor pattern with high precision and a uniform shape.
- the invention according to Claim 24 has more excellent operatability in addition to the effects of the invention according to Claim 23.
- the invention according to Claim 25 has excellent property of suppressing decrease in phosphor-containing photosensitive resin composition layer thickness in addition to the effects of the invention according to Claim 23 or 24.
- the invention according to Claim 29 has excellent property of suppressing edge fusion and property of embedding in a space of a substrate having unevenness such as a substrate for PDP and can form a phosphor pattern with high precision and a uniform shape with good operatability.
- the invention according to Claim 33 has excellent property of embedding in a space of a substrate having unevenness such as a substrate for PDP and can form a phosphor pattern with high precision and a uniform shape.
- the invention according to Claim 34 has more excellent operatability in addition to the effects of the invention according to Claim 33.
- the invention according to Claim 35 has excellent property of suppressing decrease in phosphor-containing photosensitive resin composition layer thickness in addition to the effects of the invention according to Claim 33 or 34.
- the invention according to Claim 39 has excellent property of embedding in a space of a substrate having unevenness such as a substrate for PDP and can form a phosphor pattern with high precision and a uniform shape.
- the invention according to Claim 40 has more excellent operatability in addition to the effects of the invention according to Claim 39.
- the invention according to Claim 41 has excellent property of suppressing decrease in phosphor-containing photosensitive resin composition layer thickness in addition to the effects of the invention according to Claim 39 or 40.
- the inventions according to Claims 5, 11, 18, 26, 30, 36 and 42 have more excellent operatability in addition to the effects of the inventions according to Claims 2 to 4, 15 to 17, 23 to 25, 33 to 35, 39 to 41, 10 and 29.
- the inventions according to Claims 6, 12, 19, 27, 31, 37 and 43 have more excellent storage stability in addition to the effects of the inventions according to Claims 2 to 4, 15 to 17, 23 to 25, 33 to 35, 39 to 41, 10 and 29.
- the inventions according to Claims 7, 13 and 20 have excellent property of suppressing mixing of colors in addition to the effects of the inventions according to Claims 2 to 4, 15 to 17 and 10.
- the inventions according to Claims 8 and 21 have more excellent operatability in addition to the effects of the inventions according to Claims 2 to 4 and 15 to 17.
- the inventions according to Claims 9, 14 and 22 can form a phosphor pattern with high precision and a uniform shape and have the effects of the inventions according to Claims 2 to 4, 15 to 17 and 10.
- the inventions according to Claims 28, 32 and 38 can form a phosphor pattern with high precision and a uniform shape and have the effects of the inventions according to Claims 23 to 25, 33 to 35 and 29.
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Gas-Filled Discharge Tubes (AREA)
- Formation Of Various Coating Films On Cathode Ray Tubes And Lamps (AREA)
- Photosensitive Polymer And Photoresist Processing (AREA)
- Laminated Bodies (AREA)
Applications Claiming Priority (11)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP830696 | 1996-01-22 | ||
JP830696 | 1996-01-22 | ||
JP830796 | 1996-01-22 | ||
JP8008307A JPH09199027A (ja) | 1996-01-22 | 1996-01-22 | 蛍光体パターンの製造法 |
JP964396 | 1996-01-23 | ||
JP8009644A JPH09199030A (ja) | 1996-01-23 | 1996-01-23 | 感光性エレメント及びこれを用いた蛍光体パターンの製造法 |
JP964396 | 1996-01-23 | ||
JP964496 | 1996-01-23 | ||
JP4122996 | 1996-02-28 | ||
JP4122996 | 1996-02-28 | ||
EP97100866A EP0785565A1 (fr) | 1996-01-22 | 1997-01-21 | Motif de matériau luminescent, procédés pour sa fabrication et élément photosensible utilisé |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP97100866A Division EP0785565A1 (fr) | 1996-01-22 | 1997-01-21 | Motif de matériau luminescent, procédés pour sa fabrication et élément photosensible utilisé |
Publications (1)
Publication Number | Publication Date |
---|---|
EP1387384A1 true EP1387384A1 (fr) | 2004-02-04 |
Family
ID=27518926
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP97100866A Withdrawn EP0785565A1 (fr) | 1996-01-22 | 1997-01-21 | Motif de matériau luminescent, procédés pour sa fabrication et élément photosensible utilisé |
EP03024548A Withdrawn EP1387384A1 (fr) | 1996-01-22 | 1997-01-21 | Motif de matériau luminescent,procédés pour sa fabrication et élément photosensible utilisé |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP97100866A Withdrawn EP0785565A1 (fr) | 1996-01-22 | 1997-01-21 | Motif de matériau luminescent, procédés pour sa fabrication et élément photosensible utilisé |
Country Status (3)
Country | Link |
---|---|
US (3) | US6329111B1 (fr) |
EP (2) | EP0785565A1 (fr) |
KR (2) | KR100228966B1 (fr) |
Families Citing this family (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0865067B1 (fr) * | 1997-03-11 | 2002-11-27 | Hitachi Chemical Co., Ltd. | Procédés pour la fabrication d'un motif de matériau luminescent |
EP0872870A3 (fr) * | 1997-04-14 | 1999-05-06 | Hitachi Chemical Co., Ltd. | Configuration fluorescente, procédé pour sa fabrication, solution organique alcaline pour le développement de celle-ci, émulsion de développement pour sa formation et plaque arrière pour panneau à plasma l'utilisant |
EP0887833B1 (fr) * | 1997-05-22 | 2006-08-16 | Hitachi Chemical Co., Ltd. | Procédé pour préparer un motif luminescent pour un panneau d'affichage à effet de champ et élément photosensible |
TW416086B (en) * | 1998-03-18 | 2000-12-21 | Nippon Synthetic Chem Ind | Forming method of fluorescent pattern and plasma display panel |
US7090890B1 (en) * | 1998-04-13 | 2006-08-15 | The Trustees Of Princeton University | Modification of polymer optoelectronic properties after film formation by impurity addition or removal |
JP2001043796A (ja) * | 1999-07-30 | 2001-02-16 | Sony Corp | 感熱性転写フィルム及びその使用方法 |
FR2797991A1 (fr) * | 1999-09-01 | 2001-03-02 | Thomson Plasma | Panneau d'affichage au plasma a contraste et colorimetrie ameliorees et procede fabrication d'un tel panneau |
JP4282518B2 (ja) * | 2004-03-22 | 2009-06-24 | 東京応化工業株式会社 | 感光性絶縁ペースト組成物、およびそれを用いた感光性フィルム |
KR100590008B1 (ko) * | 2004-05-18 | 2006-06-14 | 삼성에스디아이 주식회사 | 플라즈마 디스플레이 패널 및 그 제조방법 |
JP2006128048A (ja) * | 2004-11-01 | 2006-05-18 | Fujitsu Hitachi Plasma Display Ltd | Pdpの蛍光体ペースト塗布方法 |
US20060154180A1 (en) * | 2005-01-07 | 2006-07-13 | Kannurpatti Anandkumar R | Imaging element for use as a recording element and process of using the imaging element |
KR100708706B1 (ko) * | 2005-08-03 | 2007-04-17 | 삼성에스디아이 주식회사 | 플라즈마 디스플레이 패널 |
US7833442B2 (en) * | 2005-12-21 | 2010-11-16 | Essilor International (Compagnie Generale D'optique) | Method for coating an ophthalmic lens within an injection molding machine |
US7759433B2 (en) * | 2007-06-20 | 2010-07-20 | Essilor International (Compagnie Generale D'optique) | High adhesion acrylate coating for a photochromic ophthalmic lens |
FR2963112B1 (fr) * | 2010-07-21 | 2013-02-15 | Commissariat Energie Atomique | Microstructure a parois a propriete optique determinee et procede de realisation de microstructures |
JP5746553B2 (ja) * | 2011-04-28 | 2015-07-08 | 株式会社東芝 | 基板加工システム、および基板加工プログラム |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01272027A (ja) * | 1988-04-20 | 1989-10-31 | Fujitsu Ltd | ガス放電パネルの製造方法 |
EP0382260A2 (fr) * | 1989-02-10 | 1990-08-16 | Dai Nippon Insatsu Kabushiki Kaisha | Panneau d'affichage à plasma et son procédé de fabrication |
JPH04322036A (ja) * | 1991-04-19 | 1992-11-12 | Noritake Co Ltd | 蛍光面の形成方法 |
JPH06243789A (ja) * | 1993-02-15 | 1994-09-02 | Dainippon Printing Co Ltd | プラズマディスプレイパネル |
JPH07272630A (ja) * | 1994-03-30 | 1995-10-20 | Dainippon Printing Co Ltd | プラズマディスプレイパネルの蛍光面形成方法 |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3463686A (en) * | 1965-09-08 | 1969-08-26 | Sylvania Electric Prod | Cathodoluminescent screens and fabrication thereof |
JP2774277B2 (ja) | 1987-10-28 | 1998-07-09 | 大日本印刷株式会社 | 多色螢光面形成方法 |
JPH01124930A (ja) | 1987-11-09 | 1989-05-17 | Dainippon Printing Co Ltd | 螢光面形成方法 |
JPH01124929A (ja) | 1987-11-09 | 1989-05-17 | Dainippon Printing Co Ltd | 螢光面形成方法 |
JP2692908B2 (ja) | 1988-12-07 | 1997-12-17 | 大日本印刷株式会社 | プラズマディスプレイパネルおよびその蛍光面形成方法 |
DE4202282A1 (de) * | 1991-01-29 | 1992-08-20 | Fuji Photo Film Co Ltd | Lichtempfindliches uebertragungsmaterial und bilderzeugungsverfahren |
JPH0580503A (ja) * | 1991-06-25 | 1993-04-02 | Fuji Photo Film Co Ltd | 感光性転写材料及び画像形成方法 |
US5601468A (en) * | 1991-10-14 | 1997-02-11 | Dai Nippon Printing Co., Ltd. | Plasma display panel and method for forming fluorescent screens of the same |
JPH05109358A (ja) * | 1991-10-15 | 1993-04-30 | Nissha Printing Co Ltd | 蛍光膜形成方法 |
JP2552605B2 (ja) * | 1992-02-28 | 1996-11-13 | 日本写真印刷株式会社 | 蛍光膜基板の製造方法 |
JP3153043B2 (ja) | 1993-03-22 | 2001-04-03 | 日本合成化学工業株式会社 | フォトレジストフィルム |
US5858616A (en) * | 1995-10-13 | 1999-01-12 | Hitachi Chemical Company, Ltd. | Photosensitive resin composition, photosensitive film and process for preparing fluorescent pattern using the same, and phosphor subjected to surface treatment and process for preparing the same |
-
1997
- 1997-01-21 EP EP97100866A patent/EP0785565A1/fr not_active Withdrawn
- 1997-01-21 EP EP03024548A patent/EP1387384A1/fr not_active Withdrawn
- 1997-01-22 US US08/787,112 patent/US6329111B1/en not_active Expired - Fee Related
- 1997-01-22 KR KR1019970001768A patent/KR100228966B1/ko not_active IP Right Cessation
-
1999
- 1999-03-27 KR KR1019990010648A patent/KR100301914B1/ko not_active IP Right Cessation
-
2001
- 2001-08-13 US US09/927,548 patent/US6416931B2/en not_active Expired - Fee Related
-
2002
- 2002-06-11 US US10/166,079 patent/US20030090193A1/en not_active Abandoned
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01272027A (ja) * | 1988-04-20 | 1989-10-31 | Fujitsu Ltd | ガス放電パネルの製造方法 |
EP0382260A2 (fr) * | 1989-02-10 | 1990-08-16 | Dai Nippon Insatsu Kabushiki Kaisha | Panneau d'affichage à plasma et son procédé de fabrication |
JPH04322036A (ja) * | 1991-04-19 | 1992-11-12 | Noritake Co Ltd | 蛍光面の形成方法 |
JPH06243789A (ja) * | 1993-02-15 | 1994-09-02 | Dainippon Printing Co Ltd | プラズマディスプレイパネル |
JPH07272630A (ja) * | 1994-03-30 | 1995-10-20 | Dainippon Printing Co Ltd | プラズマディスプレイパネルの蛍光面形成方法 |
Non-Patent Citations (5)
Title |
---|
FUJII H ET AL: "A SANDBLASTING PROCESS FOR FABRICATION OF COLOR PDP PHOSPHOR SCREENS", SID INTERNATIONAL SYMPOSIUM DIGEST OF PAPERS, BOSTON, MAY 17 - 22, 1992, no. VOL. 23, 17 May 1992 (1992-05-17), SOCIETY FOR INFORMATION DISPLAY, pages 728 - 731, XP000479113 * |
PATENT ABSTRACTS OF JAPAN vol. 014, no. 038 (E - 878) 24 January 1990 (1990-01-24) * |
PATENT ABSTRACTS OF JAPAN vol. 017, no. 160 (E - 1342) 29 March 1993 (1993-03-29) * |
PATENT ABSTRACTS OF JAPAN vol. 018, no. 623 (E - 1635) 28 November 1994 (1994-11-28) * |
PATENT ABSTRACTS OF JAPAN vol. 096, no. 002 29 February 1996 (1996-02-29) * |
Also Published As
Publication number | Publication date |
---|---|
KR100228966B1 (ko) | 1999-11-01 |
US6416931B2 (en) | 2002-07-09 |
KR100301914B1 (ko) | 2001-09-22 |
US20030090193A1 (en) | 2003-05-15 |
EP0785565A1 (fr) | 1997-07-23 |
US6329111B1 (en) | 2001-12-11 |
KR970059843A (ko) | 1997-08-12 |
US20020018946A1 (en) | 2002-02-14 |
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